{{Rsnum
|rsid=312262787
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GGA)
|geno3=(GGA;GGA)
|Gene=SPG11
|position=44564700
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TTCC
|CHROM=15
|CLNACC=RCV000034256.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44856898_44856899insTCC
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|Disease=Spastic paraplegia 11
|FwdALT=GGA
|REF=T
|RSPOS=44856898
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=312262787
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
}}{{PMID Auto
|PMID=19196735
|Title=Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum.
}}