TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 AlteredExpression disease BEFREE Mice with a coronary artery disease-linked mutation in Wnt-coreceptor LRP6 (LDL receptor-related protein 6) exhibit vascular smooth muscle cell dedifferentiation and obstructive coronary artery disease, which are paradoxically associated with reduced TCF7L2 expression. 30567484 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 Biomarker disease CTD_human Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247 2016
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 Biomarker disease BEFREE Impaired LRP6-TCF7L2 Activity Enhances Smooth Muscle Cell Plasticity and Causes Coronary Artery Disease. 26489464 2015
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease BEFREE Moreover, we observed associations between TCF7L2 variants and the following diabetic complications: diabetic retinopathy, cardiovascular disease and coronary artery disease. 22843023 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282 2011
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease BEFREE This study aimed to evaluate the association between TCF7L2 polymorphism rs7903146 and coronary artery disease in diabetic and non-diabetic subjects. 19924244 2009
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease LHGDN TCF7L2 rs7903146 T allele is associated with a 1.57 increased risk for type 2 diabetes in a Brazilian cohort of patients with known coronary heart disease. 19055834 2008
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.450 GeneticVariation disease BEFREE TCF7L2 rs7903146 T allele is associated with a 1.57 increased risk for type 2 diabetes in a Brazilian cohort of patients with known coronary heart disease. 19055834 2008