Normal allele: TT
The TCF7L2 gene polymorphism confers an increased risk of early impaired glucose metabolism, impaired insulin secretion induced by glucagon-like peptide-1.
Polymorphism rs7901695 is related to topics like this:
Research and publications:
17245407 TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden
17668382 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium
17786212 Heterogeneity in meta-analyses of genome-wide association investigations
17971425 Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans
18533027 Worldwide population differentiation at disease-associated SNPs
18650481 TCF7L2 variants associate with CKD progression and renal function in population-based cohorts
18655717 Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population
18780302 Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.
19161620 An open access database of genome-wide association results
19207020 Meta-analysis in genome-wide association studies
19323962 Genome-wide association studies in type 2 diabetes
19602701 Underlying genetic models of inheritance in established type 2 diabetes associations
19734549 Ranking of genome-wide association scan signals by different measures
19750184 Genome-wide association studies for atherosclerotic vascular disease and its risk factors.
19913122 ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
19924244 TCF7L2 polymorphism rs7903146 is associated with coronary artery disease severity and mortality.
20144327 A genomics study of type 2 diabetes mellitus in U.S. Air Force personnel
20816152 Obesity and diabetes genetic variants associated with gestational weight gain.
20862305 Identification of new genetic risk variants for type 2 diabetes.
20886378 Physiologic characterization of type 2 diabetes-related loci
21036813 A variable selection method for genome-wide association studies.
21133856 Genome-wide association scan allowing for epistasis in type 2 diabetes.
21278902 Genetic risk profiling for prediction of type 2 diabetes
21297524 The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations.
21507254 Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease.
22584884 The effect of type 2 diabetes risk loci on insulin requirements in type 1 diabetes.
23073174 From genotype to human β cell phenotype and beyond
23386860 Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.
23456907 Maternal genotype and gestational diabetes
23577239 Genetics of obesity and type 2 diabetes in African Americans.
25477898 Replication of obesity and diabetes-related SNP associations in individuals from Yucatán, México.
25774817 Genetics of type 2 diabetes-pitfalls and possibilities.
26648684 Update on genetics and diabetic retinopathy.
27153677 Assessing statistical significance in multivariable genome wide association analysis.
27383215 Type 2 Diabetes Risk Allele Loci in the Qatari Population.
27730450 Candidate gene studies of diabetic retinopathy in human.
28002648 Association between TCF7L2 polymorphisms and gestational diabetes mellitus: A meta-analysis.