rs12255372, TCF7L2

N. diseases: 28
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.900 SusceptibilityMutation CLINVAR
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE Recently, the transcription factor 7-like 2 (TCF7L2) gene on chromosome 10q25.2 has been linked with type 2 diabetes among Caucasians, with disease associations noted for single nucleotide polymorphisms (SNPs) rs12255372 and rs7903146. 17130514 2006
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE A total of 2,676 healthy European white middle-aged men from the prospective NPHSII (158 developed T2D over 15 years surveillance) were genotyped for two intronic SNPs [rs 7903146 (IVS3C>T) and rs12255372 (IVS4G>T)] which showed strong linkage disequilibrium (D' = 0.88, p<0.001; R(2)=0.76, p<0.001). 17665514 2006
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE In a prospective, nested, case-control study (n = 3,520) within the Nurses' Health Study (687 type 2 diabetic case and 1,051 control subjects) and the Health Professionals Follow-up Study (886 case and 896 control subjects), we examined the association of a common variant of the TCF7L2 gene (rs12255372 [T/G]) with type 2 diabetes risk among Caucasians. 16936216 2006
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE We compared genotype frequencies in subjects with type 2 diabetes with those with NGT and found marginal association for rs7901695 (P = 0.05; odds ratio [OR] 1.51); comparison between NGT control subjects and the combined type 2 diabetes/IGT case group showed strong association with rs7901695 and rs7903146 (P = 0.008-0.01; OR 1.53-1.57) and marginal association with rs11196205 and rs12255372 (P = 0.07 and P = 0.04, respectively). 16936218 2006
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE Both the T-allele of rs7903146 and the T-allele of rs12255372 significantly increase type 2 diabetes risk with an allelic odds ratio (OR) of 1.69 (95% CI 1.55-1.83) (P = 6.0 x 10(-35)) and 1.60 (1.47-1.74) (P = 7.6 x 10(-28)), respectively. 17003360 2006
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.090 GeneticVariation BEFREE We examined whether the two most strongly associated variants (rs12255372 and rs7903146) predict the progression to diabetes in persons with impaired glucose tolerance who were enrolled in the Diabetes Prevention Program, in which lifestyle intervention or treatment with metformin was compared with placebo. 16855264 2006
Diabetes
CUI: C0011847
Disease: Diabetes
0.090 GeneticVariation BEFREE We examined whether the two most strongly associated variants (rs12255372 and rs7903146) predict the progression to diabetes in persons with impaired glucose tolerance who were enrolled in the Diabetes Prevention Program, in which lifestyle intervention or treatment with metformin was compared with placebo. 16855264 2006
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
0.030 GeneticVariation BEFREE We examined whether the two most strongly associated variants (rs12255372 and rs7903146) predict the progression to diabetes in persons with impaired glucose tolerance who were enrolled in the Diabetes Prevention Program, in which lifestyle intervention or treatment with metformin was compared with placebo. 16855264 2006
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
0.030 GeneticVariation BEFREE We genotyped four of the SNPs (rs7901695, rs7903146, rs11196205, and rs12255372) in Amish subjects with type 2 diabetes (n = 137), impaired glucose tolerance (IGT; n = 139), and normal glucose tolerance (NGT; n = 342). 16936218 2006
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
0.010 GeneticVariation BEFREE Our results suggest a possible influence of TCF7L2 rs12255372 on the risk of familial BC. 17109766 2006
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE Furthermore, we identified a common protective haplotype defined by these four SNPs that was significantly associated with type 2 diabetes and age at diagnosis (P = 4.2 x 10(-5), relative risk [RR] 0.69; P = 6.7 x 10(-6), respectively) and a haplotype that confers diabetes risk that contains the rare alleles at SNPs rs10885390 and rs12255372 (P = 0.02, RR 1.64). 17259383 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation GWASDB A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE The previously reported SNPs rs7903146 T- and rs12255372 T-alleles of the TCF7L2 gene were rare and were not associated with type 2 diabetes in a Chinese population, which may attribute to the low frequencies of these two SNPs. 17579206 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE Here, we report replication of association between T2D and three SNPs in the case-control (rs7901695, P=0.003; rs7901346, P=0.00002; and rs12255372, P=0.000004) and two SNPs in the family-based (rs7901695, P=0.01 and rs7901346, P=0.04) samples from northern Sweden. 17245407 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE In a population-based cohort of elderly men with well-defined phenotypes and biochemical markers related to type 2 diabetes mellitus, we analysed two single nucleotide polymorphisms (SNPs), rs7903146 and rs12255372, in the transcription factor 7-like 2 gene (TCF7L2), which are associated with an increased risk of type 2 diabetes mellitus. 17618413 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE In conclusion, the T allele of the rs12255372(G/T) and rs7903146(C/T) polymorphisms of TCF7L2 gene confer susceptibility to type 2 diabetes mellitus in Asian Indians. 17697858 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation GWASDB Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. 17668382 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE Results of our analyses strongly confirmed the minor T alleles as risk variants for type 2 diabetes (rs7903146: OR (TvsC) [95% CI]=1.36 [1.18;1.58], p=0.00003, and rs12255372: OR (TvsG) [95% CI]=1.31 [1.13;1.51], p=0.0003). 17226113 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation GWASDB A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. 17460697 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE The variant of rs12255372 of TCF7L2 was associated with incident type 2 diabetes in the DPS and in a separate population-based cross-sectional study. 17437080 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE We observed a significant association between the single-nucleotide polymorphism (SNP) rs12255372 and the microsatellite DG10S478 with T2D in the Mexican sample [rs12255372, odds ratio (OR) = 1.78, p = 0.017; DG10S478, OR = 1.62, p = 0.041]. 17470138 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE We genotyped 6,516 participants for rs12255372 and rs7903146 and analysed the role in type 2 diabetes susceptibility using binary logistic regression. 17429603 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE The rest of the five SNPs (rs7895340, rs11196205 and rs12255372) did not show any significant associations with type 2 diabetes. 17245589 2007