List of variants in gene HADH, LOC129992931 studied 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
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005327.4(HADH):c.-71C>T	rs760202	0.02185
NM_005327.4(HADH):c.-193G>A	rs10017687	0.02168
NM_005327.4(HADH):c.-65G>A	rs28703310	0.01115
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
NC_000004.12:g.107986495_107992009del
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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