ClinVar Miner

List of variants in gene CCNO reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_021147.5(CCNO):c.685G>A (p.Gly229Ser)	rs139980939	0.00052
NM_021147.5(CCNO):c.16C>A (p.Pro6Thr)	rs1299342018	0.00003

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