{{Rsnum
|rsid=118203986
|Gene=CCT5
|Chromosome=5
|position=10256063
|Orientation=plus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CCT5
}}{{omim
|id=610150
|rsnum=118203986
|variant=0001
}}{{ClinVar
|rsid=118203986
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=10256175
|CHROM=5
|GMAF=0
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=CCT5:22948
|GENE_NAME=CCT5
|GENE_ID=22948
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.10256175A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610150.0001
|CLNSIG=5
|CLNCUI=C1850395
|CLNDBN=Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive
|Disease=Neuropathy
|CLNACC=RCV000001390.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850395:256840:139578
|COMMON=0
}}