List of variants in gene C2 reported as 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_000063.6(C2):c.1023G>A (p.Ala341=)	rs1042663	0.11857
NM_000063.6(C2):c.954G>C (p.Glu318Asp)	rs9332739	0.03307

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