{{Rsnum
|rsid=312262744
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=SPG11
|position=44621906
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TA
|CHROM=15
|CLNACC=RCV000001172.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44914104_44914105insA
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1210; 610844.0005
|Disease=Spastic paraplegia 11
|FwdALT=T
|REF=T
|RSPOS=44914104
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262744
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=18067136
|Title=Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
}}