DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Cardiomyopathy, Dilated ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557315928
rs1557315928
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0007193
Disease:
Cardiomyopathy, Dilated 		T 0.700 CausalMutation CLINVAR