ClinVar Miner

List of variants in gene combination HADH, LOC129992931 reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005327.4(HADH):c.-193G>A	rs10017687	0.02168
NM_005327.4(HADH):c.-65G>A	rs28703310	0.01115

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