Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917757
rs121917757
HRAS ; LRRC56
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism 		0.010 GeneticVariation BEFREE A previously reported individual with the rare HRAS p.Gln22Lys had hyperinsulinemic hypoglycemia. 26572961

2016