rs57965306, DES

N. diseases: 6
Disease: Paresis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Paresis
CUI: C0030552
Disease: Paresis
0.010 GeneticVariation BEFREE Our study documents distinct signs of normal and R349P mutant desmin-related remodeling of the 3D myofibrillar architecture during aging, which provides a structural basis for the progressive muscle weakness. 28715662 2017