List of variants in gene ANKRD1 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_014391.2(ANKRD1):c.-145T>C	rs10881855	0.67382
NM_014391.3(ANKRD1):c.*59A>G	rs3939	0.38933
NM_014391.3(ANKRD1):c.346-15_346-14insA	rs60700562	0.01084
NM_014391.3(ANKRD1):c.-17A>G	rs79341122	0.00753
NM_014391.3(ANKRD1):c.348G>A (p.Thr116=)	rs137914723	0.00748
NM_014391.3(ANKRD1):c.148G>C (p.Ala50Pro)	rs28730751	0.00387
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00269
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244
NM_014391.3(ANKRD1):c.208-16C>T	rs79793575	0.00161
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln)	rs150797476	0.00092
NM_014391.3(ANKRD1):c.417C>A (p.Phe139Leu)	rs201398260	0.00043
NM_014391.3(ANKRD1):c.108T>C (p.Ala36=)	rs145211719	0.00009
NM_014391.3(ANKRD1):c.346-14_346-9del	rs773314113
NM_014391.3(ANKRD1):c.346-15_346-14del	rs794728971
NM_014391.3(ANKRD1):c.346-17_346-10del	rs397517250
NM_014391.3(ANKRD1):c.346-19_346-14del	rs58762441
NM_014391.3(ANKRD1):c.346-19_346-18del	rs398014415
NM_014391.3(ANKRD1):c.346-21ATTT[2]	rs397517250
NM_014391.3(ANKRD1):c.346-29_346-12del	rs72003210

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