{{Rsnum
|rsid=199588440
|Gene=SPG11
|Chromosome=15
|position=44628785
|Orientation=plus
|GMAF=0.0004591
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A
|CAF=0.9995; 0.0004591
|CHROM=15
|CLNACC=RCV000034185.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44920983G>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|COMMON=0
|Disease=Spastic paraplegia 11
|FwdALT=A
|FwdREF=G
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
|REF=G
|RSPOS=44920983
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000016110100
|WGT=0
|dbSNPBuildID=137
|rsid=199588440
}}{{PMID Auto
|PMID=18067136
|Title=Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
}}

{{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.
}}