NKX2-5, NK2 homeobox 5, 1482

N. diseases: 165; N. variants: 55
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893907
rs104893907
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
CUI: C3276096
Disease:
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104893907
rs104893907
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
CUI: C3276096
Disease:
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		C 0.700 CausalMutation CLINVAR