ClinVar Miner

List of variants in gene HADH reported as likely risk allele 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.275T>G (p.Phe92Cys)	rs61735992	0.00516
NM_005327.7(HADH):c.587del (p.Ser196fs)	rs745727504

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