{{Rsnum
|rsid=149003934
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SPG11
|position=44573595
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000034242.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44865793C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdALT=T
|FwdREF=C
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
|REF=C
|RSPOS=44865793
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=149003934
}}{{PMID Auto
|PMID=19196735
|Title=Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum.
}}