TCF21, transcription factor 21, 6943

N. diseases: 143; N. variants: 6
Disease: Congenital heart 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: C0152021
Disease:
Congenital heart disease 		0.010 GeneticVariation BEFREE However, whether rs12190287 polymorphisms in the TCF21-3'UTR confer predisposition to congenital heart disease (CHD) is unclear. 28346832 2017