List of variants in gene HADH 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005327.7(HADH):c.257T>C (p.Leu86Pro)	rs4956145	0.86661
NM_005327.7(HADH):c.-38T>C	rs17550794	0.13904
NM_005327.7(HADH):c.257= (p.Leu86=)	rs4956145	0.13339
NM_005327.7(HADH):c.*109T>A	rs221347	0.07950
NM_005327.7(HADH):c.636+13G>A	rs17511214	0.04139
NM_005327.4(HADH):c.*818A>G	rs17511319	0.03973
NM_005327.7(HADH):c.881A>G (p.Asn294Ser)	rs36030668	0.00738
NM_005327.7(HADH):c.662G>A (p.Arg221His)	rs76476980	0.00358
NM_005327.7(HADH):c.*514A>G	rs183594888	0.00020
NM_005327.7(HADH):c.133-15C>T	rs190144364	0.00013
NM_005327.7(HADH):c.261+16C>T	rs71601073

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