List of variants in gene ANKRD11 reported as benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn)	rs201636725	0.00654
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser)	rs145906515	0.00377
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=)	rs146025366	0.00285
NM_013275.6(ANKRD11):c.5661A>G (p.Gln1887=)	rs147726863	0.00185
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys)	rs202081612	0.00121
NM_013275.6(ANKRD11):c.2519G>A (p.Arg840Gln)	rs149776253	0.00070
NM_013275.6(ANKRD11):c.5481C>G (p.Pro1827=)	rs142469039	0.00041
NM_013275.6(ANKRD11):c.5178C>T (p.Ser1726=)	rs200783129	0.00020

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