{{Rsnum
|rsid=312262746
|Chromosome=15
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SPG11
|position=44620327
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000034197.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44912525C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=44912525
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=312262746
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=19105190
|Title=Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
}}