rs225014, DIO2

N. diseases: 22
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 Our results indicate that in a case-control study, the homozygosity for D2 Thr92Ala polymorphism is associated with increased risk for DM2. 20566590 2010