{{Rsnum
|rsid=66468541
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HSPD1
|position=197497275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSPD1
}}{{omim
|id=118190
|rsnum=66468541
|variant=0001
}}{{ClinVar
|rsid=66468541
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=198361999
|CHROM=2
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HSPD1:3329
|GENE_NAME=HSPD1
|GENE_ID=3329
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.198361999C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=118190.0001
|CLNSIG=5
|CLNCUI=C1854467
|CLNDBN=Spastic paraplegia 13
|Disease=Spastic paraplegia 13
|CLNACC=RCV000019112.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1854467:605280:100994
}}