{{Rsnum
|rsid=80338869
|Gene=SPG11
|Chromosome=15
|position=44564675
|Orientation=minus
|GMAF=0.01286
|Gene_s=SPG11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=A,T
|CAF=0.9871; 0.01286; .
|CHROM=15
|CLNACC=RCV000034258.2; RCV000034257.2
|CLNALLE=1; 2
|CLNDBN=Spastic paraplegia 11, autosomal recessive
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1210:C1858479:604360
|CLNHGVS=NC_000015.9:g.44856873G>A; NC_000015.9:g.44856873G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1210
|COMMON=1
|Disease=Spastic paraplegia 11
|FwdALT=A,T
|FwdREF=C
|GENEINFO=SPG11:80208
|GENE_ID=80208
|GENE_NAME=SPG11
|REF=G
|RSPOS=44856873
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000140416110100
|WGT=0
|dbSNPBuildID=132
|rsid=80338869
}}{{PMID Auto
|PMID=19105190
|Title=Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
}}