Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893642
rs104893642
0.710 GeneticVariation BEFREE A novel T608R missense mutation in insulin receptor substrate-1 identified in a subject with type 2 diabetes impairs metabolic insulin signaling. 12679424

2003

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE To assess the relevance of a Gly-->Arg substitution in codon 972 of the insulin receptor substrate-1 gene in impaired glucose tolerance (IGT) and NIDDM. 9589236

1998

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Thus, our data suggest that the common T2D susceptibility polymorphism of TCF7L2 (rs7903146 C/T) gene, and the G972R polymorphism of the IRS1 gene, seem to predispose to GDM in Greek women. 20540670

2011

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE The aim of our study was to investigate whether common polymorphisms in the genes regulating the early insulin signalling pathway (insulin; A-23T, insulin-like growth factor 1 receptor [IGF-1R]; GAG1013GAA, plasma cell membrane glycoprotein 1 [PC-1]; K121Q, insulin receptor substrate [IRS-1]; G972R, insulin receptor substrate 2 [IRS-2]; G1057D and phosphatidylinositol 3-kinase p85 alpha [PI3K]; M326I) affect the weight change and development of Type 2 diabetes in the Finnish Diabetes Prevention Study. 15127203

2004

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Gly972Arg is more common than other known mutations in our population but may not be a major determinant in genetic susceptibility to type 2 diabetes. 16284438

2005

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Gly971Arg, is more common in Mexican Americans and Caucasians, but is not a major contributor to genetic susceptibility to Type 2 diabetes. 11025561

2000

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Our findings revealed that IRS-1 Gly972Arg and IRS-2 Gly1057Asp polymorphisms are associated with T2DM in the Kurdish ethnic group. 22994406

2012

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Several polymorphisms in the IRS genes have been identified, but only the Gly-->Arg972 substitution of IRS-1, interacting with environmental factors, seems to have a pathogenic role in the development of type 2 diabetes. 11641236

2001

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE IRS1 G972R polymorphism and type 2 diabetes: a paradigm for the difficult ascertainment of the contribution to disease susceptibility of 'low-frequency-low-risk' variants. 19557384

2009

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE The most commonly detected polymorphism in human insulin receptor substrate-1 (IRS-1), a glycine to arginine change at codon 972 (G972R), is associated with an increased risk of Type 2 diabetes and insulin resistance. 15590636

2005

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE These alterations may account for the increased predisposition to type 2 diabetes in individuals carrying the Gly(972)-->Arg amino acid polymorphism of IRS-1. 11978638

2002

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE We studied possible relations between GDM and both insulin receptor substrate 1 (IRS-1) (Gly972Arg) and beta3-adrenergic receptor (ADRB3 Trp64Arg, beta3-AR) gene mutations, considered potential modifying factors in the etiology of type 2 diabetes mellitus. 17046546

2006

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE We replicated the significant association of rs1801278 and rs3792267 SNPs of the IRS1 and CAPN10 genes with T2DM in the population of Hyderabad. 24612564

2014

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE The purpose of this study was to examine the role of the IRS-1 missense mutations at codons 972 (glycine to arginine) and 513 (alanine to proline) in two diverse populations from South India and Finland at high risk for NIDDM. 7796990

1995

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Gly971Arg of IRS-1 gene does not play an important role in the development of NIDDM in this population. 8732707

1996

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE This meta-analysis suggests that rs1801278 may play a role in type 2 diabetes risk, especially in Asian. 26582067

2016

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Also, the diagnostic test to exclude diabetes amongst control subjects interacted with the association between the IRS-1 Gly972Arg variant and Type 2 diabetes (p=0.03). 12819898

2003

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE The Gly972Arg mutation in the IRS-1 gene has been found to be associated with insulin resistance and type II diabetes. 12588284

2003

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE This study confirms in a large and ethnically homogeneous sample that IRS1 G972R polymorphism is associated with failure to OAD among patients with T2D. 24947357

2014

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Association of Gly972Arg polymorphism of IRS1 gene with type 2 diabetes mellitus in lean participants of a national health survey in Mexico: a candidate gene study. 19716569

2010

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Two SSCP variants that change the sequence of the protein, delta S686/687 (deletion of the codons for serine-686 and 687) and G972R, were identified in two different NIDDM subjects, both whom were also heterozygous for the V101I polymorphisms in GLUT2. 7713316

1995

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Our findings indicate that the IRS-1 Gly972Arg variant does not substantially increase risk of common Type 2 diabetes, or Type 2 diabetes in obese persons. 15209769

2004

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE In all, though further studies are needed for confirming this finding, our present data point to IRS1 rs1801278 as a potential biomarker for pursuing the goal of stratified medicine in the field of antihyperglycemic treatment in T2D. 28696414

2018

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE By using a Cox proportional hazard model, common variants in the PPARG (P12A), CAPN10 (SNP43 and 44), KCNJ11 (E23K), UCP2 (-866G>A), and IRS1 (G972R) genes were studied for their ability to predict T2D in 2,293 individuals participating in the Botnia study in Finland. 17570749

2005

dbSNP: rs1801278
rs1801278
0.100 GeneticVariation BEFREE Insulin resistance and glucose dysmetabolism in polycystic ovary syndrome (PCOS) are related with the polymorphisms in the genes encoding the insulin receptor substrate (IRS) proteins, especially Gly972Arg/Ala513Pro polymorphism being reported to be associated with type-2 diabetes and PCOS. 16603055

2006