Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE KCNQ1 polymorphism at SNPs rs151290 and rs2237895 is strongly associated with CVD in this population, but presented no association with T2D. 28863213

2019
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE In conclusions, rs151290 (KCNQ1) polymorphisms are associated with increased risk of T2DM, alone and especially in interaction with smoking and alcohol. 28806535

2017
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE Consistent with results of genotype analysis, the C allele of rs151290 in KCNQ1 was also associated with increased risk of T2DM (OR = 1.166, 95% CI = 1.004-1.355, p = 0.045). 26927145

2016
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE The risk allele C of rs151290 in KCNQ1 and risk allele G of rs972283 in KLF14 were both associated with increased risk of T2DM in a global population. 24486580

2014
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE We found that all the genotyped KCNQ1 variants were significantly associated with type 2 diabetes in our Dutch population, and the association of rs151290 was the strongest (OR 1.20, 95% CI 1.07-1.35, p = 0.002). 22403629

2012
dbSNP: rs151290
rs151290
KCNQ1
0.060 GeneticVariation BEFREE We genotyped 1,578 nondiabetic subjects at increased risk of type 2 diabetes for rs151290, rs2237892, rs2237895, and rs2237897. 19366866

2009