Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE For TCF7L2, the rs11196218 genotype GA and the haplotype CCG, TTG, TTA were associated with T2DM risk; whereas, the haplotype CTG and TCG were associated with decreased risk. 26083111

2015

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE The combined analysis indicated that the rs11196218A/G polymorphism was not associated with type 2 diabetes mellitus</span> (G vs. A, OR=1.04,</span> 95% CI=0.97-1.13, p=0.28). 26247673

2015

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE The rs11196218(IVS4G>A) and rs290487 (IVS3C>T) SNPs were not associated with T2DM risk. 23311683

2013

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE In addition, no significant associations were found between the two polymorphisms (rs290487 and rs11196218) and type 2 diabetes. 23188737

2013

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE There was no significant association between rs11196218 and T2D. 22245614

2012

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE We analyzed single nucleotide polymorphisms (SNPs) rs11196218 and rs290487 of the TCF7L2 gene, which showed robust associations with T2D in Chinese population, in 430 PCOS patients and 360 control subjects by pyrosequencing, and also assessed the effect of genotype on clinical and biochemical traits in the PCOS group. 22296403

2012

dbSNP: rs11196218
rs11196218
0.100 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: rs11196218
rs11196218
0.100 GeneticVariation BEFREE Novel risk loci for type 2 diabetes, single nucleotide polymorphism (SNP) rs7756992 in cyclin-dependent kinase 5 (CDK5) regulatory subunit associated protein 1-like 1 (CDKAL1), rs290487 and rs11196218 in transcription factor 7-like 2 (TCF7L2), were recently identified. 19718565

2010

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE Perform the meta-analysis of all the validated studies and evaluate the association between rs7903146 T allele, rs12255372 T allele, rs11196205 C allele, rs290487 C allele and rs11196218 G allele of TCF7L2 and the risk of T2DM. 19482368

2009

dbSNP: rs11196218
rs11196218
0.100 GeneticVariation BEFREE Interestingly, another SNP (rs11196218 G allele) located in adjacent LD block conferred independent risk for T2D [OR (95%CI) =1.43 (1.14-1.79)] and contributed high-population attributable risk of 42%. 17609304

2007