List of variants reported as uncertain significance for Hyperinsulinemic hypoglycemia, familial, 1 by New York Genome Center

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.3112G>A (p.Asp1038Asn)	rs367974472	0.00010
NM_000352.6(ABCC8):c.375C>G (p.His125Gln)	rs60637558	0.00008
NM_000352.6(ABCC8):c.647G>A (p.Arg216His)	rs199702708	0.00006
NM_000352.6(ABCC8):c.1067A>G (p.Tyr356Cys)	rs59852838	0.00005
NM_000352.6(ABCC8):c.1537G>A (p.Ala513Thr)	rs761748692	0.00005
NM_000352.6(ABCC8):c.4412-4T>G	rs1476016104	0.00002
NM_000352.6(ABCC8):c.250G>A (p.Val84Ile)	rs775776658	0.00001
NM_000352.6(ABCC8):c.3661C>T (p.Arg1221Trp)	rs567382793	0.00001
NM_000352.6(ABCC8):c.1012-7C>G
NM_000352.6(ABCC8):c.1332+3A>G
NM_000352.6(ABCC8):c.1468-52G>A
NM_000352.6(ABCC8):c.1571C>T (p.Thr524Met)
NM_000352.6(ABCC8):c.1672-473T>G
NM_000352.6(ABCC8):c.1913A>C (p.Tyr638Ser)
NM_000352.6(ABCC8):c.2105G>A (p.Arg702His)
NM_000352.6(ABCC8):c.2684A>T (p.His895Leu)
NM_000352.6(ABCC8):c.3928G>T (p.Ala1310Ser)
NM_000352.6(ABCC8):c.421G>A (p.Val141Met)

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