Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10248619
rs10248619
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1305855
Disease:
Body mass index 		0.800 GeneticVariation GWASDB A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs10248619
rs10248619
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1305855
Disease:
Body mass index 		T 0.800 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs12540874
rs12540874
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0036421
Disease:
Systemic Scleroderma 		0.800 GeneticVariation GWASCAT Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181 2011
dbSNP: rs12540874
rs12540874
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0036421
Disease:
Systemic Scleroderma 		0.800 GeneticVariation GWASDB Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181 2011
dbSNP: rs10486757
rs10486757
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11555134
rs11555134
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs145761614
rs145761614
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17152083
rs17152083
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0017654
Disease:
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs2237467
rs2237467
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0005612
Disease:
Birth Weight 		A 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs2529411
rs2529411
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2715135
rs2715135
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs6976572
rs6976572
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs73116822
rs73116822
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0017654
Disease:
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs73116829
rs73116829
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs9656664
rs9656664
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17548938
rs17548938
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs17548938
rs17548938
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0200638
Disease:
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10275663
rs10275663
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1305849
Disease:
Diastolic blood pressure measurement 		0.700 GeneticVariation GWASCAT Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study. 25189868 2015
dbSNP: rs10275663
rs10275663
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0428883
Disease:
Diastolic blood pressure 		0.700 GeneticVariation GWASCAT Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study. 25189868 2015
dbSNP: rs933360
rs933360
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C0202098
Disease:
Insulin measurement 		A 0.700 GeneticVariation GWASCAT A central role for GRB10 in regulation of islet function in man. 24699409 2014
dbSNP: rs933360
rs933360
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C4049919
Disease:
Insulin Sensitivity Measurement 		A 0.700 GeneticVariation GWASCAT A central role for GRB10 in regulation of islet function in man. 24699409 2014
dbSNP: rs12540874
rs12540874
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		G 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs4245555
rs4245555
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		G 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs4245556
rs4245556
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		T 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs4947709
rs4947709
Entrez Id: 2887
Gene Symbol: GRB10
GRB10
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013