DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Muscular Dystrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556962271
rs1556962271
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease:
Muscular Dystrophy 		AAATG 0.700 GeneticVariation CLINVAR