Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514580
rs397514580
GCK ; LOC105375258
CUI: C0020456
Disease: Hyperglycemia
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