List of variants in gene HADH reported as benign for Hyperinsulinemic hypoglycemia, familial, 4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.-38T>C	rs17550794	0.13904
NM_005327.7(HADH):c.*109T>A	rs221347	0.07950
NM_005327.4(HADH):c.*818A>G	rs17511319	0.03973
NM_005327.7(HADH):c.662G>A (p.Arg221His)	rs76476980	0.00358

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