List of variants reported as likely risk allele for Hyperinsulinemic hypoglycemia

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.99C>G (p.Ile33Met)	rs74428123	0.00038
NM_005327.7(HADH):c.908G>T (p.Gly303Val)	rs575378007	0.00005
NM_005327.7(HADH):c.761A>G (p.Tyr254Cys)	rs771071992	0.00001
NM_005327.7(HADH):c.118G>A (p.Ala40Thr)	rs137853101
NM_005327.7(HADH):c.725A>G (p.Glu242Gly)	rs1736337186

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