ClinVar Miner

List of variants in gene PROC reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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.479G>C (p.Cys160Ser)	rs1450037999	0.00001
NM_000312.4(PROC):c.1155G>A (p.Met385Ile)	rs1688692415

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