List of variants reported as likely pathogenic for Hyperinsulinemic hypoglycemia, familial, 4

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.662G>A (p.Arg221His)	rs76476980	0.00358
NM_005327.7(HADH):c.706C>T (p.Arg236Ter)	rs375717077	0.00003
NM_005327.7(HADH):c.100G>C (p.Gly34Arg)	rs779135938
NM_005327.7(HADH):c.261+1G>A	rs1398546361
NM_005327.7(HADH):c.434C>A (p.Ala145Asp)
NM_005327.7(HADH):c.587del (p.Ser196fs)	rs745727504

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