List of variants in gene ANKRD1 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00240
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.368C>T (p.Thr123Met)	rs145387010	0.00030
NM_014391.3(ANKRD1):c.196C>G (p.Arg66Gly)	rs397517249
NM_014391.3(ANKRD1):c.346-13_346-12del
NM_014391.3(ANKRD1):c.346-13_346-12dup	rs766545285
NM_014391.3(ANKRD1):c.346-17_346-12del	rs1564574609
NM_014391.3(ANKRD1):c.346-19_346-15delinsA	rs2492960517
NM_014391.3(ANKRD1):c.346-21ATTT[2]	rs397517250
NM_014391.3(ANKRD1):c.346-43AT[14]	rs60406118
NM_014391.3(ANKRD1):c.454-16A>T	rs1022005009

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