Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Diabetes mellitus autosomal dominant type II (disorder)
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
0.700 CausalMutation CLINVAR
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
0.010 GeneticVariation BEFREE In the present study, we identified and functionally characterized a novel missense mutation in the GCK gene, which results in a protein mutation Glu(339)→Lys (E339K), from a Chinese family with hyperglycemia. 21104275 2011