List of variants in gene combination HADH, LOC129992931 reported as benign for Deficiency of 3-hydroxyacyl-CoA dehydrogenase

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_005327.4(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

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