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rs771251369

From SNPedia

ClinVar
Risk rs771251369(;)
Alt rs771251369(;)
Reference rs771251369(AGA;AGA)
Significance Pathogenic
Disease Persistent hyperinsulinemic hypoglycemia of infancy not provided
Variation info
Gene ABCC8
CLNDBN Persistent hyperinsulinemic hypoglycemia of infancy not provided
Reversed 0
HGVS NC_000011.9:g.17417435_17417437delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000177757.2, RCV000201913.1,