DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Proximal muscle weakness in lower limbs ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886043676
rs886043676
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1866010
Disease:
Proximal muscle weakness in lower limbs 		A 0.700 CausalMutation CLINVAR