List of variants in gene combination HADH, LOC129992931 reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005327.4(HADH):c.-51delC	rs574132278	0.00074
NM_005327.4(HADH):c.-115delG	rs537335460	0.00053
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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