List of variants in gene ANKRD1 reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 3

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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.560C>T (p.Ser187Phe)	rs397517251	0.00001

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