List of variants in gene CCNO reported as likely benign for CCNO-related disorder

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_021147.5(CCNO):c.957G>A (p.Lys319=)	rs7712656	0.00273
NM_021147.5(CCNO):c.354G>A (p.Pro118=)	rs368155527	0.00139
NM_021147.5(CCNO):c.999C>T (p.His333=)	rs143418535	0.00003

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