DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Mitochondrial DNA mutation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769985775
rs769985775
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0948444
Disease:
Mitochondrial DNA mutation 		0.010 GeneticVariation BEFREE All patients with MIDD were confirmed as carrying the m.3243A>G mitochondrial DNA mutation. 28599824 2017