List of variants in gene C6 reported as likely pathogenic for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000065.5(C6):c.2381+2T>C	rs76202909	0.00242
NM_000065.5(C6):c.821del (p.Gln274fs)	rs557023458	0.00131
NM_000065.5(C6):c.1786C>T (p.Arg596Ter)	rs142881576	0.00013
NM_000065.5(C6):c.928-1G>C	rs1432520854	0.00001
NM_000065.5(C6):c.1628_1629dup (p.Gln544fs)
NM_000065.5(C6):c.2049C>G (p.Tyr683Ter)	rs867425110
NM_000065.5(C6):c.2101C>A (p.Arg701=)
NM_000065.5(C6):c.2335_2336del (p.Gln779fs)	rs771792933
NM_000065.5(C6):c.2406_2407del (p.Val802_Phe803insTer)	rs749432203
NM_000065.5(C6):c.2624-1G>A

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