List of variants in gene combination HADH, LOC129992931 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005327.4(HADH):c.-102G>A	rs182097151	0.00354
NM_005327.4(HADH):c.-203A>G	rs376591232	0.00049
NM_005327.4(HADH):c.-86G>T	rs528952923	0.00001
NM_005327.4(HADH):c.-195A>C	rs886058979
NM_005327.4(HADH):c.-195A>G	rs886058979
NM_005327.4(HADH):c.-56C>A	rs770197760

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