List of variants in gene CCNF reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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_001761.3(CCNF):c.1885G>A (p.Val629Met)	rs541386499	0.00001
NM_001761.3(CCNF):c.329A>G (p.Tyr110Cys)	rs200331327	0.00001
NM_001761.3(CCNF):c.71G>A (p.Arg24Lys)	rs2065260644

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