TCF21, transcription factor 21, 6943

N. diseases: 143; N. variants: 6
Disease: Ventricular Septal Defects ×
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: C0018818
Disease:
Ventricular Septal Defects 		0.010 GeneticVariation BEFREE Our results demonstrate that rs12190287 polymorphisms confer predisposition to VSDs in the Chinese population studied here. 28346832 2017