TCF21, transcription factor 21, 6943

N. diseases: 143; N. variants: 6
Disease: Coronary Artery Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C1956346
Disease:
Coronary Artery Disease 		0.720 GeneticVariation BEFREE Functional rs12190287 polymorphisms located within the 3' untranslated region (3'-UTR) of TCF21 were associated with a risk of coronary heart disease in the European and Eastern populations. 28346832 2017
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C1956346
Disease:
Coronary Artery Disease 		0.720 GeneticVariation BEFREE Our data provide the first evidence for the association of miR-146a rs2910164 and TCF21 rs12190287 with CAD in an Iranian population, encouraging further research to elucidate the disease-related effects of miR-146a rs2910164. 26909569 2016
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C1956346
Disease:
Coronary Artery Disease 		G 0.720 GeneticVariation GWASDB Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C1956346
Disease:
Coronary Artery Disease 		0.720 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125 2013
dbSNP: rs2327429
rs2327429
Entrez Id: 6943;100507308
Gene Symbol: TCF21;TARID
TCF21;TARID
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018