List of variants in gene C9 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001737.5(C9):c.1451T>A (p.Met484Lys)	rs145969667	0.00109
NM_001737.5(C9):c.1585G>A (p.Ala529Thr)	rs137891079	0.00028
NM_001737.5(C9):c.376G>A (p.Gly126Arg)	rs199939436	0.00017
NM_001737.5(C9):c.355T>G (p.Cys119Gly)	rs121909593	0.00013
NM_001737.5(C9):c.409G>A (p.Glu137Lys)	rs753246845	0.00002
NM_001737.5(C9):c.1346T>C (p.Val449Ala)
NM_001737.5(C9):c.1677del (p.Lys559fs)	rs762159491

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