Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Overall, the E23K variant was found to be significantly associated with Type II diabetes (0.001 < or = p < or = .00106, corrected p-values for multiple testing p < or = 0.01). 9867219

1998

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE In the present study, the association of the E23K polymorphism with type 2 diabetes was not significant (P = 0.26). 12540638

2003

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Meta-analysis of all case-control data showed that the E23K all</span>ele was associated with type 2 diabetes (K allele OR 1.23 [1.12-1.36], P = 0.000015; KK genotype 1.65 [1.34-2.02], P = 0.000002); but the ABCC8 variants were not associated. 12540637

2003

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE We have genotyped three single nucleotide polymorphisms associated with type 2 diabetes in a large type 1 diabetic family collection of European descent: Gly972Arg in the insulin receptor substrate 1 (IRS1) gene, Glu23Lys in the potassium inwardly-rectifying channel gene (KCNJ11), and Pro12Ala in the peroxisome proliferative-activated receptor gamma2 gene (PPARG2). 14988278

2004

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE We conclude that the polymorphisms of the SUR1 gene predicted the conversion from impaired glucose tolerance to type 2 diabetes and that the effect of these polymorphisms on diabetes risk was additive with the E23K polymorphism of the Kir6.2 gene. 15579791

2004

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE We show that E23K is also associated with decreased insulin secretion in glucose-tolerant control subjects, supporting a mechanism whereby beta-cell dysfunction contributes to the common form of type 2 diabetes. 15111507

2004

dbSNP: rs5219
rs5219
0.900 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: rs5219
rs5219
0.900 GeneticVariation BEFREE In conclusion, our results showed no evidence of a synergistic interaction between the KCNJ11 Glu(23)Lys and PPARG Pro(12)Ala polymorphisms, but indicated that they may act in an additive manner to increase the risk of type 2 diabetes. 15797964

2005

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE These variants may contribute significantly to the risk type 2 diabetes conferring insulin resistance of liver, muscle and fat (Pro12Ala) and a relative insulin secretory deficiency (Glu23Lys). 15715885

2005

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE The common KCNJ11 E23K gene variant, but not the ABCC8 exon 16 or exon 18 variant, was consistently associated with Type 2 diabetes. 15842514

2005

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE These data suggest that the E23K variant in KCNJ11 may influence the variability in the response of patients to sulfonylureas, thus representing an example of pharmacogenetics in type 2 diabetes. 16595597

2006

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Our data indicate that HNF4A P2 promoter polymorphisms may interact with KCNJ11 E23K in predicting Type 2 diabetes in women. 17894829

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Given the phenotypic overlap between PCOS and T2D, we investigated whether E23K is involved in susceptibility to PCOS and related traits. 17342155

2007

dbSNP: rs5219
rs5219
T 0.900 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

dbSNP: rs5219
rs5219
T 0.900 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

dbSNP: rs5219
rs5219
T 0.900 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program. 17259403

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE A meta-analysis of East Asian studies, comprising a total of 3,357 T2D patients (77.4% Japanese) and 2,836 control subjects (77.8% Japanese), confirmed the significant role of the KCNJ11 E23K variant in T2D susceptibility. 17823772

2007

dbSNP: rs5219
rs5219
T 0.900 GeneticVariation GWASDB A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE All the polymorphic loci in KCNJ11 are in strong linkage disequilibrium in the Korean population and act as one haplotype block. g.67G>A and g.1009A>G were associated with an increased risk of Type 2 diabetes [age, sex, and body mass index (BMI)-adjusted odds ratios (OR) = 1.376 (1.085-1.745), P = 0.008 and 1.411 (1.111-1.791), P = 0.005, respectively], as was one haplotype (A-T-A-C-G-C in the order of polymorphisms as shown above) containing g.67A and g.1009G [OR = 1.359 (1.080-1.709), P = 0.009]. 17257281

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE The polymorphism E23K on KCNJ11 that is associated with NIDDM was differentially distributed in the 2 cohorts. 17727257

2007

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE Given the phenotypic overlap between PCOS and T2DM, our objective was to investigate whether the TCF7L2 rs7903146(C/T) and the KCNJ11 E23K variants are involved in susceptibility to PCOS and related traits in a Greek population. 18958766

2008

dbSNP: rs5219
rs5219
0.900 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: rs5219
rs5219
0.900 GeneticVariation BEFREE The P12A variant in the PPARG gene and the E23K polymorphism in KCNJ11 are both known to influence individual predisposition to type 2 diabetes. 17994213

2008

dbSNP: rs5219
rs5219
0.900 GeneticVariation BEFREE The aim of this study was to investigate the association of KCNJ11 E23K and ABCC8 exon16-3T/C with the therapeutic effect of repaglinide in patients with type 2 diabetes. 18664331

2008