{{Rsnum
|rsid=267607084
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SPG11
|position=44663530
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000001170.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44955728G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1210; 610844.0003
|Disease=Spastic paraplegia 11
|FwdALT=T
|FwdREF=C
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
|REF=G
|RSPOS=44955728
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607084
}}{{PMID Auto
|PMID=17322883
|Title=Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
}}

{{PMID Auto
|PMID=18079167
|Title=Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
}}