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
1.000 GeneticVariation BEFREE <b>Conclusion:</b> The present meta-analysis demonstrated that <i>SLC30A8</i> rs13266634 was a potential risk factor for T2DM, and more studies should be performed to confirm the association between rs13266634 polymorphism and IGR. 30319545

2018

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A case-control study was performed in Han Chinese subjects with normal control (n=152) and T2DM (n=227), we genotyped rs7903146 and rs11196218 at TCF7L2, rs13266634 at SLC30A8, rs3811951 at PCSK1 and rs2021785 at PCSK2. 21437630

2012

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A common variant W325R in the C-terminal domain (CTD) increases the risk to develop type 2 diabetes and affects autoantibody specificity in type 1 diabetes. 29430817

2018

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A non-synonymous polymorphism (R325W) in its gene is associated with Type-2 diabetes. 30710592

2019

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A nonsynonymous single nucleotide polymorphism rs13266634 in the SLC30A8 gene, encoding the secretory granule zinc transporter ZnT8, is associated with type 2 diabetes. 19542200

2009

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 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 A specific genetic variant, rs13266634 (c.973C>T; p.ARG325TRP) in zinc transporter SLC30A8/ZnT8, is associated with protection against Type-2 Diabetes, suggesting it may be actionable for predicting and preventing POHG. 31220282

2019

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE A total of 556 healthy controls and 413 T2DM patients were genotyped for ZnT8 Arg325Trp polymorphism confirming the association of Arg-325 variant with an increased T2DM risk (OR = 1.35 95% C.I: 1.10-1.66; p = 0.0044). 30142362

2018

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE After excluding four SNPs due to Hardy-Weinberg disequilibrium, significant associations in age-matched cohorts were found betweenT2DM and the following SNPs: rs9939609 (FTO), rs13266634 (SLC30A8), rs7961581 (TSPAN8/LGR5), and rs1799883 (FABP2). 28738793

2017

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Although previous meta-analyses have shown that this association was only found in Asian and European groups, and not in African populations, our analysis revealed the deleterious effect of SLC30A8 rs13266634 on T2DM in an African population when stratified by ethnicity under additive model even with a small number of studies. 26832344

2016

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 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 Association to type 2 diabetes was found for rs13266634 (SLC30A8), rs7923837 (HHEX), rs10811661 (CDKN2A/2B), rs4402960 (IGF2BP2), rs12779790 (CDC123/CAMK1D), and rs2237892 (KCNQ1). 22923468

2012

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE For this reason, the present study looked at the contribution of ENNP1 (rs1044498), IGF2BP2 (rs1470579), KCNJ11 (rs5219), MLXIPL (rs7800944), PPARγ (rs1801282), SLC30A8 (rs13266634) and TCF7L2 (rs7903146) SNPs to the risk of T2DM in Lebanese and Tunisian Arabs. 22749234

2012

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Gene-environment interaction analysis showed a significant interaction between rs13266634</span> in SLC30A8 gene and age on T2DM risk (P<0.0001). 24736664

2014

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

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
1.000 GeneticVariation BEFREE In addition, we also confirmed that three SNPs (rs1111875, rs7923837 and rs5015480) in HHEX , one SNP (rs10946398) in CDKAL1, and three SNPs (rs13266634, rs3802177 and rs11558471) in SLC30A8 were significantly associated with T2D in the population being studied. 20550665

2010

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE In Chinese Han, we replicated the associations between 7 genetic loci and T2D, with risk allele-specific odds ratios (ORs) as follows: 1.27 (95% CI, 1.11-1.45; p = 0.0008) for CDKAL1-rs10946398, 1.26 (95% CI, 1.08-1.47; p = 0.003) for IGF2BP2-rs4402960, 1.19 (95% CI, 1.04-1.37; p = 0.009) for SLC30A8-rs13266634, 1.22 (95% CI, 1.06-1.41; p = 0.005) for CDKN2A/B-rs10811661, 1.20 (95% CI, 1.01-1.42; p = 0.03) for HHEX-rs5015480, 1.37 (95% CI, 1.19-1.69; p = 1.0 x 10(-4)) for KCNQ1-rs2237892, and 1.24 (95% CI, 1.01-1.52; p = 0.046) for FTO-rs8050136 after adjustment for age, gender, and body mass index. 20509872

2010

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 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 Meanwhile PPARG-2 Pro12Ala, CDKN2A/2B rs10811661, IGF2BP2 rs4402960, HHEX rs7923837, CDKAL1 rs7754840, EXT2 rs1113132 and SLC30A8 rs13266634 were found to have no significant association with T2D among Arabs. 23458876

2013

dbSNP: rs13266634
rs13266634
Diabetes Mellitus, Non-Insulin-Dependent
1.000 GeneticVariation BEFREE Nine variants in FTO rs8050136, WFS1 rs10010131, CDKN2A/B rs10811661, KCNJ11 rs5219, CDC123/CAMK1D rs12779790, JAZF1 rs864745, SLC30A8 rs13266634, CDKAL1 rs10946398, and HHEX/IDE rs5015480 were significantly associated with T2DM (P < 0.05). 23298195

2013

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