Variant: rs7901695 

    present in Gene: TCF7L2
    present in Chromosome: 10
    Position on Chromosome: 112994329
    Alleles of this Variant: T/C

rs7901695 in TCF7L2 gene and Coronary Artery Disease PMID 29212778 2018 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

rs7901695 in TCF7L2 gene and Coronary heart disease PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs7901695 in TCF7L2 gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 17463249 2007 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.

PMID 30718926 2019 Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.

PMID 20818381 2010 A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.

PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

PMID 23670970 2013 Genetic modifiers of cystic fibrosis-related diabetes.

PMID 17668382 2007 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.