List of variants in gene HADH reported as pathogenic 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.706C>T (p.Arg236Ter)	rs375717077	0.00003
NM_005327.7(HADH):c.547-3_549del	rs2126234459
NM_005327.7(HADH):c.636+471G>T	rs786200932
NM_005327.7(HADH):c.773C>T (p.Pro258Leu)	rs137853103

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