List of variants in gene PROC reported as likely benign for Thrombophilia due to protein C deficiency, autosomal recessive; Thrombophilia due to protein C deficiency, autosomal dominant

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.1212G>A (p.Gly404=)	rs370637632	0.00016
NM_000312.4(PROC):c.927C>T (p.Ala309=)	rs200731614	0.00011
NM_000312.4(PROC):c.-21-37G>A
NM_000312.4(PROC):c.-21-74C>T

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