List of variants in gene ANKRD17 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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_032217.5(ANKRD17):c.5135G>A (p.Arg1712His)	rs139064430	0.00002
NM_032217.5(ANKRD17):c.1927G>A (p.Val643Ile)	rs2531069593
NM_032217.5(ANKRD17):c.344A>C (p.Asn115Thr)	rs906955660

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