List of variants in gene C5 reported as likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001735.3(C5):c.4679-2A>G	rs191466386	0.00004
NM_001735.3(C5):c.1407G>A (p.Trp469Ter)	rs1408798589	0.00001
NM_001735.3(C5):c.2257+1G>A	rs750416999	0.00001
NM_001735.3(C5):c.4336del (p.Val1446fs)	rs1554718962

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