Normal allele: AA
A common variant of the TCF7L2 gene is closely associated with type 2 diabetes mellitus.
Polymorphism rs4506565 is related to topics like this:
Research and publications:
18224312 Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment
18655717 Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population
19161620 An open access database of genome-wide association results
19913122 ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
20039379 A powerful approach to sub-phenotype analysis in population-based genetic association studies.
20081858 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
20979565 Population structure of Aggarwals of north India as revealed by molecular markers.
21036813 A variable selection method for genome-wide association studies.
21217814 Presymptomatic risk assessment for chronic non-communicable diseases.
22238593 A genome-wide association search for type 2 diabetes genes in African Americans.
22971100 Quick, "imputation-free" meta-analysis with proxy-SNPs.
24128935 Impact of TCF7L2 single nucleotide polymorphisms on hydrochlorothiazide-induced diabetes.
25393876 Identification of allelic heterogeneity at type-2 diabetes loci and impact on prediction.
25477898 Replication of obesity and diabetes-related SNP associations in individuals from Yucatán, México.
25774817 Genetics of type 2 diabetes-pitfalls and possibilities.
27153677 Assessing statistical significance in multivariable genome wide association analysis.
27185397 Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases.
27383215 Type 2 Diabetes Risk Allele Loci in the Qatari Population.
29025879 TCF7L2 Genetic Variants Contribute to Phenotypic Heterogeneity of Type 1 Diabetes.
35601672 Diabetes, cigarette smoking and transcription factor 7-like 2 (Tcf7L2) in the UK Biobank cohort.