{{Rsnum
|rsid = 17860403
|Gene = CASP10
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=2
|position=201208114
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASP10
}}{{omim
|desc=AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA
|id=601762
|rsnum=17860403
|variant=0001
}}

{{ClinVar
|rsid=17860403
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=202072837
|CHROM=2
|dbSNPBuildID=123
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=CASP10:843
|GENE_NAME=CASP10
|GENE_ID=843
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.202072837C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1108; 601762.0001
|CLNSIG=5
|CLNCUI=C1858968; C1858968
|CLNDBN=Autoimmune lymphoproliferative syndrome, type 2
|Disease=Autoimmune lymphoproliferative syndrome
|CLNACC=RCV000008205.1
|Tags=PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1108:C1858968:603909:3261
}}

{{PMID Auto
|PMID=10412980
|Title=Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}