List of variants in gene C1S reported as likely benign for immune system disorder

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_001734.5(C1S):c.979G>C (p.Val327Leu)	rs2239170	0.00032
NM_001734.5(C1S):c.622T>C (p.Leu208=)	rs144205018	0.00006

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