List of variants in gene C1QB reported as uncertain significance 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.217G>A (p.Gly73Arg)	rs35477594	0.00054
NM_001378156.1(C1QB):c.371C>A (p.Ala124Asp)
NM_001378156.1(C1QB):c.623G>A (p.Gly208Asp)

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