DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Muscle Weakness ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518962
rs1057518962
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0151786
Disease:
Muscle Weakness 		T 0.700 CausalMutation CLINVAR