DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Atrial Septal Defects ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886042604
rs886042604
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0018817
Disease:
Atrial Septal Defects 		G 0.700 CausalMutation CLINVAR