Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9989419
rs9989419
0.700 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

dbSNP: rs998451
rs998451
0.700 GeneticVariation GWASDB Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. 23209189

2013

dbSNP: rs997509
rs997509
0.010 GeneticVariation BEFREE In conclusion, we found a new SNP, rs99</span>7509, in intron 1 that is strongly associated with risk of type 2 diabetes in obese individuals. 16936213

2006

dbSNP: rs9973676
rs9973676
0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444

2017

dbSNP: rs9966620
rs9966620
A 0.700 GeneticVariation GWASCAT A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity. 31264924

2019

dbSNP: rs9966483
rs9966483
0.010 GeneticVariation BEFREE Here we investigated the association of POL1-nearby variant rs488846, MALT1-nearby variant rs2874116, MC4R-nearby variant rs1942872, PHLPP rs9958800 and DSEL-nearby variant rs9966483 single nucleotide polymorphisms (SNPs) in the 18q region, previously linked with DN in African-Americans, with T2DM in (North African) Tunisian subjects, followed by their association with DN, which was performed subsequent to the analysis of the association with T2DM. 23727064

2013

dbSNP: rs995922697
rs995922697
0.010 GeneticVariation BEFREE The presence of Pro197Leu substitution of the GPx-1 gene may play a crucial role in determining genetic susceptibility to coronary-arteriosclerosis in T2D. 17825092

2007

dbSNP: rs9958800
rs9958800
0.010 GeneticVariation BEFREE Here we investigated the association of POL1-nearby variant rs488846, MALT1-nearby variant rs2874116, MC4R-nearby variant rs1942872, PHLPP rs9958800 and DSEL-nearby variant rs9966483 single nucleotide polymorphisms (SNPs) in the 18q region, previously linked with DN in African-Americans, with T2DM in (North African) Tunisian subjects, followed by their association with DN, which was performed subsequent to the analysis of the association with T2DM. 23727064

2013

dbSNP: rs995447
rs995447
G 0.700 GeneticVariation GWASDB Genetic modifiers of cystic fibrosis-related diabetes. 23670970

2013

dbSNP: rs994965583
rs994965583
G 0.700 GeneticVariation GWASCAT Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population. 30130595

2018

dbSNP: rs994411260
rs994411260
0.010 GeneticVariation BEFREE In our study, GAS6 intron 8 c.834 + 7G > A polymorphism was not associated with diabetic nephropathy in type 2 diabetes mellitus. 25869052

2015

dbSNP: rs9942471
rs9942471
0.710 GeneticVariation BEFREE Analysis of specific DKD phenotypes identified a novel signal near <i>GABRR1</i> (rs9942471, <i>P</i> = 4.5 × 10<sup>-8</sup>) associated with microalbuminuria in European T2D case subjects. 29703844

2018

dbSNP: rs9942471
rs9942471
A 0.710 GeneticVariation GWASCAT Analysis of specific DKD phenotypes identified a novel signal near <i>GABRR1</i> (rs9942471, <i>P</i> = 4.5 × 10<sup>-8</sup>) associated with microalbuminuria in European T2D case subjects. 29703844

2018

dbSNP: rs9940149
rs9940149
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018

dbSNP: rs9940149
rs9940149
G 0.700 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590

2017

dbSNP: rs9940128
rs9940128
FTO
0.010 GeneticVariation BEFREE among South Indians, the rs9940128 A/G, rs11076023 A/T, and rs1588413 C/T variants of the FTO gene were associated with T2DM, whereas the rs8050136 C/A variant was associated with obesity. 21175269

2011

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE The minor allele (T) in rs9939609 was significantly higher (P=0.0001) in T2DM (31.25%) when compared with that of the control obese group (20%). 28603074

2017

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE Variants (such as rs9939609) in the fat mass- and obesity-associated (FTO) gene have been associated with obesity, type 2 diabetes, some cancers, and alcohol consumption. 23771786

2013

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE This was a cross-sectional study of 236 patients with type 2 diabetes (age 60.0 ± 10.3 years; diabetes duration 12.7 ± 8.2 years; 53.4% females) who were genotyped for FTO rs9939609. 23689376

2013

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE We investigated the association between genetic variants in FTO (rs9939609) and near MC4R (rs17782313) with obesity- and type 2 diabetes (T2DM)-related traits in a longitudinal birth cohort of 2,151 healthy individuals from the Vellore birth cohort in South India. 22421923

2012

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE We investigated potential interactions between body mass index (BMI) and genotypes of human leukocyte antigen (HLA), TCF7L2-rs7903146, and FTO-rs9939609 in relation to the risk of latent autoimmune diabetes in adults (LADA) and type 2 diabetes. 31125083

2019

dbSNP: rs9939609
rs9939609
FTO
A 0.900 GeneticVariation GWASCAT Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. 22693455

2012

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation GWASDB Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. 22158537

2011

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE The increased fat mass in carriers of the A allele of rs9939609 of FTO is associated not only with increased risk of type 2 diabetes, but also with an increase in atherogenic lipid profile and myocardial infarction in these patients. 20031593

2009

dbSNP: rs9939609
rs9939609
FTO
0.900 GeneticVariation BEFREE Recent genome-wide association studies have showed that common variant (rs9939609) in fat mass and obesity associated (FTO) gene was significantly associated with type 2 diabetes through an effect on human body mass index/obesity. 22311015

2012