DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Creatine phosphokinase serum increased ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039785
rs886039785
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0241005
Disease:
Creatine phosphokinase serum increased 		T 0.700 GeneticVariation CLINVAR