Disease: Dystrophia myotonica 2 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
0.010 GeneticVariation BEFREE Several investigations in animal models demonstrate the protective role of MT in DM2 and its cardiovascular or renal complications, while a copious literature shows that a common polymorphism (R325W) in ZnT8, which affects the protein's zinc transport activity, is associated with increased DM2 risk. 28845600 2017