List of variants in gene C1QB reported as pathogenic 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_001378156.1(C1QB):c.523C>T (p.Arg175Ter)	rs751172449	0.00001
NM_001378156.1(C1QB):c.724G>A (p.Gly242Arg)	rs34813378	0.00001
NM_001378156.1(C1QB):c.181+1G>T	rs1361922961

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