List of variants in gene combination ABCC8, LOC110121471 reported as uncertain significance for Hyperinsulinemic hypoglycemia, familial, 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2389C>T (p.Arg797Trp)	rs142620721	0.00006
NM_000352.6(ABCC8):c.2350GAG[1] (p.Glu785del)
NM_000352.6(ABCC8):c.2454_2456del (p.Asp818_Gln819delinsGlu)	rs1554916621

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