{{Rsnum
|rsid=119477056
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CD96
|position=111585362
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CD96
}}{{omim
|id=606037
|rsnum=119477056
|variant=0002
}}{{ClinVar
|rsid=119477056
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=111304209
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CD96:10225
|GENE_NAME=CD96
|GENE_ID=10225
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000003.11:g.111304209C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606037.0002
|CLNSIG=5
|CLNCUI=C0796095
|CLNDBN=C syndrome
|Disease=C syndrome
|CLNACC=RCV000004903.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796095:211750:1308
}}