{{Rsnum
|rsid=281865117
|Orientation=minus
|Chromosome=13
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=SACS
|position=23335032
|Gene_s=SACS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000005847.2
|CLNALLE=1
|CLNDBN=Spastic ataxia Charlevoix-Saguenay type
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1255:C1849140:270550:98
|CLNHGVS=NC_000013.10:g.23909171delA
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1255; 604490.0001
|Disease=Spastic ataxia Charlevoix-Saguenay type
|FwdREF=T
|REF=TA
|RSPOS=23909170
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281865117
|GENEINFO=SACS:26278
|GENE_ID=26278
|GENE_NAME=SACS
}}{{PMID Auto
|PMID=10655055
|Title=ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF.
}}