{{Rsnum
|rsid=80358239
|Gene=CASP10
|Chromosome=2
|position=201209363
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CASP10
}}{{omim
|id=601762
|rsnum=80358239
|variant=0007
}}{{ClinVar
|rsid=80358239
|Reversed=0
|FwdREF=A
|FwdALT=C,T
|REF=A
|ALT=C,T
|RSPOS=202074086
|CHROM=2
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000040016110100
|GENEINFO=CASP10:843
|GENE_NAME=CASP10
|GENE_ID=843
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.202074086A>C
|CLNORIGIN=0
|CLNSRCID=
NBK1108; 601762.0007
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000008211.1
|Tags=PM;PMC;S3D;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDBN=Autoimmune lymphoproliferative syndrome, type 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1108:C1858968:603909:3261
|CLNSRC=GeneReviews; OMIM Allelic Variant
|COMMON=1
|Disease=Autoimmune lymphoproliferative syndrome
}}{{PMID Auto
|PMID=10412980
|Title=Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II.
}}

{{PMID Auto
|PMID=16446975
|Title=Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome.
}}