ClinVar Miner

List of variants in gene PROC reported as likely pathogenic by Genetics and Molecular Pathology, SA Pathology

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_000312.4(PROC):c.565C>T (p.Arg189Trp)	rs146922325	0.00026
NM_000312.4(PROC):c.962C>T (p.Pro321Leu)	rs1321566264	0.00001

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