List of variants in gene C1QA reported as uncertain significance for C1Q deficiency

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_015991.4(C1QA):c.11C>G (p.Pro4Arg)	rs149230484	0.00023
NM_015991.4(C1QA):c.162G>A (p.Pro54=)	rs375714569	0.00013
NM_015991.4(C1QA):c.470G>A (p.Gly157Asp)	rs1570073403

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