DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201217593
rs201217593
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0878544
Disease:
Cardiomyopathies
T 0.700 GeneticVariation CLINVAR