List of variants in gene C7 reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000587.4(C7):c.1341G>A (p.Glu447=)	rs150696042	0.00183
NM_000587.4(C7):c.1258A>C (p.Lys420Gln)	rs3792646	0.00103

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