List of variants in gene CASP8 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_001372051.1(CASP8):c.306-1910G>A	rs373232880	0.00002
NM_001372051.1(CASP8):c.411+1G>C	rs1948252170	0.00001
NM_001372051.1(CASP8):c.742C>T (p.Arg248Trp)	rs17860424	0.00001
NC_000002.12:g.(?_201276807)_(201276988_?)dup

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