List of variants in gene PCSK7 reported as uncertain significance for benign neoplasm

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_004716.4(PCSK7):c.1678C>G (p.Arg560Gly)	rs202038275	0.00023
NM_004716.4(PCSK7):c.1634A>C (p.Lys545Thr)	rs771986131

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