List of variants in gene ANKRD17 reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_032217.5(ANKRD17):c.2110G>T (p.Ala704Ser)	rs2148822115
NM_032217.5(ANKRD17):c.3384T>G (p.His1128Gln)
NM_032217.5(ANKRD17):c.3698C>A (p.Ala1233Asp)
NM_032217.5(ANKRD17):c.7799A>G (p.Asn2600Ser)	rs2530008604
NM_032217.5(ANKRD17):c.812T>C (p.Leu271Pro)

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