FOXP4, forkhead box P4, 116113

N. diseases: 30; N. variants: 4
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: rs1114167294
rs1114167294
Entrez Id: 116113
Gene Symbol: FOXP4
FOXP4
CUI: C0018818
Disease:
Ventricular Septal Defects 		C 0.700 GeneticVariation CLINVAR