List of variants reported as uncertain risk allele for Hyperinsulinemic hypoglycemia, familial, 1 by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2521C>T (p.Arg841Ter)	rs1484689392	0.00001
NM_000352.6(ABCC8):c.4477C>T (p.Arg1493Trp)	rs28936371	0.00001
NM_000352.6(ABCC8):c.2169_2171del (p.Leu724del)	rs760520781
NM_000352.6(ABCC8):c.4160_4162del (p.Phe1387del)	rs151344624
NM_000352.6(ABCC8):c.683G>A (p.Gly228Asp)	rs863225280

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