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

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.349G>C (p.Val117Leu)	rs146732064	0.00035
NM_005327.7(HADH):c.696G>A (p.Arg232=)	rs747476251	0.00001
NM_005327.7(HADH):c.419+39del	rs550348868
NM_005327.7(HADH):c.617del (p.Lys206fs)	rs1735963864

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