List of variants in gene C2 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000063.6(C2):c.954G>C (p.Glu318Asp)	rs9332739	0.03307
NM_000063.5(C2):c.-145A>C	rs150299426	0.00017
NM_000063.6(C2):c.1567+22_1567+43del	rs541057516

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