DES, desmin, 1674

N. diseases: 330; N. variants: 63
Disease: Myofibrillar Myopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607485
rs267607485
Entrez Id: 1674
Gene Symbol: DES
DES
CUI: C2678065
Disease:
Myofibrillar Myopathy 		C 0.700 CausalMutation CLINVAR