List of variants in gene CCDC22 reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014008.5(CCDC22):c.1070C>G (p.Thr357Ser)	rs144685788	0.00183
NM_014008.5(CCDC22):c.659G>A (p.Arg220Gln)	rs201088755	0.00025
NM_014008.5(CCDC22):c.926C>A (p.Ala309Asp)	rs183877705	0.00014
NM_014008.5(CCDC22):c.1078G>A (p.Val360Ile)	rs145766807	0.00008
NM_014008.5(CCDC22):c.1164C>T (p.Arg388=)	rs184896758	0.00008
NM_014008.5(CCDC22):c.1207C>T (p.Leu403=)	rs782089419	0.00002
NM_014008.5(CCDC22):c.81C>T (p.Arg27=)	rs370789286	0.00002
NM_014008.5(CCDC22):c.972G>C (p.Gln324His)	rs587780297	0.00001
NM_014008.5(CCDC22):c.747= (p.Gln249=)	rs2294020

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