List of variants reported as likely benign for Hyperinsulinemic hypoglycemia, familial, 1

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2390+123C>T	rs4148631	0.70926
NM_000352.6(ABCC8):c.2390+93C>T	rs4148630	0.70902
NM_000352.6(ABCC8):c.4119+93G>T	rs4148644	0.21307
NM_000352.6(ABCC8):c.4714G>A (p.Val1572Ile)	rs8192690	0.05059
NM_005327.7(HADH):c.636+13G>A	rs17511214	0.04139
NM_000352.6(ABCC8):c.2277C>T (p.Thr759=)	rs1801261	0.02724
NM_000352.6(ABCC8):c.-19A>G	rs193922394	0.01648
NM_000352.6(ABCC8):c.1158C>T (p.Asn386=)	rs60824529	0.01375
NM_000352.6(ABCC8):c.3329+6C>T	rs113873225	0.01304
NM_000352.6(ABCC8):c.4728C>T (p.Phe1576=)	rs73419228	0.01181
NM_000352.6(ABCC8):c.2538C>T (p.His846=)	rs73423037	0.01028
NM_000352.6(ABCC8):c.423G>A (p.Val141=)	rs116132921	0.01009
NM_000352.6(ABCC8):c.1572G>A (p.Thr524=)	rs61748766	0.00948
NM_000352.6(ABCC8):c.1332+4del	rs587783164	0.00128
NM_000352.6(ABCC8):c.1920G>A (p.Ala640=)	rs146156937	0.00103
NM_000352.6(ABCC8):c.3203C>T (p.Thr1068Met)	rs139524121	0.00102
NM_000352.6(ABCC8):c.1384A>G (p.Ile462Val)	rs117874766	0.00097
NM_000352.6(ABCC8):c.1063G>A (p.Ala355Thr)	rs145136257	0.00057
NM_000352.6(ABCC8):c.1678G>A (p.Val560Met)	rs4148619	0.00019
NM_000352.6(ABCC8):c.2422C>A (p.Gln808Lys)	rs202189540	0.00006
NM_000352.6(ABCC8):c.2500C>T (p.Arg834Cys)	rs140068774	0.00004
NM_000352.6(ABCC8):c.2475+19G>A	rs373894772	0.00001
NM_000352.6(ABCC8):c.602C>T (p.Pro201Leu)	rs933815442	0.00001
NM_000352.6(ABCC8):c.2062T>G (p.Trp688Gly)	rs1955658642
NM_000352.6(ABCC8):c.2256-16del	rs774508952
NM_000352.6(ABCC8):c.3435C>T (p.Ser1145=)	rs371089976

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