Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1411638309
rs1411638309
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		A 0.700 GeneticVariation CLINVAR The C terminus of SUR1 is required for trafficking of KATP channels. 10400694

1999