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 The pancreatic amyloid main component is a protein known as human islet amyloid polypeptide (hIAPP) or amylin, the most common mutation is the S20G in Asian population with a polymorphic frequency in DM2 Asian patients. 16950544 2007