Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
T 1.000 SusceptibilityMutation CLINVAR

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASDB Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASDB A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE SNPs in other genes such as rs7756992 in CDKAL1, rs10811661 in CDKN2B and rs13266634 in SLC30A8 showed nominal association with type 2 diabetes. rs7756992 in CDKAL1 and rs10811661 in CDKN2B were correlated with impaired pancreatic beta cell function as estimated by the homeostasis model assessment beta index (p = 0.023, p = 0.0083, respectively). 17928989

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE We replicated the association with type 2 diabetes for rs10811661 in the vicinity of CDKN2B (OR 1.20, 95% CI: 1.06-1.37, p=0.004), rs9939609 in FTO (OR 1.14, 95% CI: 1.04-1.25, p=0.006) and rs13266634 in SLC30A8 (OR 1.20, 95% CI: 1.09-1.33, p=3.9 x 10(-4)). 18437351

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A significant association with type 2 diabetes was not observed for rs13266634. 17971426

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Amongst non-obese individuals, we observed significant T2D associations with HNF1A I27L [odds ratio (OR) = 1.14, P = 0.04], GCK -30G>A (OR = 1.23, P = 0.01), SLC30A8 R325W (OR = 0.87, P = 0.04), and TCF7L2 rs7903146 (OR = 1.89, P = 4.5 x 10-23), and non-significant associations with PPARG Pro12Ala (OR = 0.85, P = 0.14), ADIPOQ -11,377C>G (OR = 1.00, P = 0.97) and ENPP1 K121Q (OR = 0.99, P = 0.94). 18498634

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A significant association for SNP rs13266634 was observed between patients with type 2 diabetes and NGT controls (P = 0.016). 18628523

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE When combined, each additional risk allele from CDKAL1-rs9465871, CDKN2A/B-rs10811661, IGF2BP2-rs4402960, and SLC30A8-rs13266634 increased the risk for type 2 diabetes by 1.24-fold (P = 2.85 x 10(-7)) or for combined IFG/type 2 diabetes by 1.21-fold (P = 6.31 x 10(-11)). 18633108

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Individuals carrying T2D risk alleles of CDKAL1 or SLC30A8 had lower fasting plasma insulin level (rs7756992 P = 0.003) or lower basal insulin secretion (rs13266634 P = 0.0005), respectively, than non-carriers. 18210030

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Of European non-diabetic offspring of type 2 diabetes patients, 46% are homozygous carriers of the Arg325Trp polymorphism in ZnT-8, which is known to associate with type 2 diabetes. 18324385

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Among the 11 loci examined, 6 were significantly associated with type 2 diabetes in our population by a logistic regression analysis, similar to previously reported results (rs4402960, P = 0.00009; rs10811661, P = 0.0024; rs5219, P = 0.0034; rs1111875, P = 0.0064; rs13266634, P = 0.0073; rs7756992, P = 0.0363). 18162508

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE The R325W (rs13266634) nonsynonymous polymorphism in the islet-specific zinc transporter protein gene, SLC30A8, has been reported to be associated with type 2 diabetes and possibly with a defect in insulin secretion. 18162509

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Genome-wide association scans in type 2 diabetes (T2D) have identified a risk variant, rs13266634 (Arg325Trp), in SLC30A8 on chromosome 8. 18400535

2008

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. 19401414

2009

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
C 1.000 GeneticVariation GWASCAT Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. 19734900

2009

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE In our case-control subjects, susceptibility to type 2 diabetes was replicated in TCF7L2 (rs12255372), CDKAL1 (rs7756992, rs7754840), HHEX (rs7923837), IGF2BP2 (rs4402960 and rs1470579), CDKN2A/B (rs10811661), and SLC30A8 (rs13266634). 19033397

2009

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE SLC30A8 (rs13266634) was the only type 2 diabetes variant associated with higher fasting glucose (0.033 mmol/l [0.01-0.06], P = 0.01). 19741166

2009

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Genome-wide association scans for type 2 diabetes (T2D) susceptibility loci revealed and then replicated a highly significant association between the R allele of the R325W variant of SLC30A8 (marker rs13266634) and susceptibility to T2D in Caucasians. 19655390

2009