List of variants in gene HADHA reported as benign for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000182.5(HADHA):c.573+32T>C	rs7593175	0.61061
NM_000182.5(HADHA):c.573+26G>C	rs35746418	0.17547
NM_000182.5(HADHA):c.67+51G>T	rs62128457	0.17544
NM_000182.5(HADHA):c.180+69G>C	rs2303892	0.17014
NM_000182.5(HADHA):c.474C>T (p.Tyr158=)	rs11552518	0.16973
NM_000182.5(HADHA):c.68-82T>A	rs12987980	0.16953
NM_000182.5(HADHA):c.315-44A>C	rs3892649	0.16834
NM_000182.5(HADHA):c.1072C>A (p.Gln358Lys)	rs2229420	0.02193
NM_000182.5(HADHA):c.109+20A>G	rs7569108	0.01898
NM_000182.5(HADHA):c.573+8dup	rs112196218	0.00584
NM_000182.5(HADHA):c.68-10T>G	rs144414842	0.00403
NM_000182.5(HADHA):c.567C>T (p.Pro189=)	rs183297747	0.00047
NM_000182.5(HADHA):c.67+17G>C	rs574255291	0.00001
NM_000182.5(HADHA):c.1080T>G (p.Asp360Glu)

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