List of variants in gene CFP reported as pathogenic for not provided

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_001145252.3(CFP):c.481C>T (p.Arg161Ter)	rs132630258
NM_001145252.3(CFP):c.961T>G (p.Trp321Gly)	rs1603083173
NM_001145252.3(CFP):c.985C>T (p.Arg329Ter)	rs1603083122

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