List of variants in gene ANKRD11 reported as uncertain significance by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)	rs201589586	0.00023
NM_013275.6(ANKRD11):c.2213G>A (p.Arg738His)	rs370690185	0.00009
NM_013275.6(ANKRD11):c.3343A>G (p.Ile1115Val)	rs753868881	0.00002
NM_013275.6(ANKRD11):c.1994A>G (p.Lys665Arg)	rs769640583	0.00001
NM_013275.6(ANKRD11):c.6046C>T (p.Pro2016Ser)	rs1449729767	0.00001
NM_013275.6(ANKRD11):c.6377G>A (p.Gly2126Asp)	rs763100566	0.00001
NM_013275.6(ANKRD11):c.6704C>T (p.Pro2235Leu)	rs1394383095	0.00001
NM_013275.6(ANKRD11):c.149A>T (p.Glu50Val)	rs1567614253
NM_013275.6(ANKRD11):c.6159G>C (p.Ala2053=)	rs368315956

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