{{Rsnum
|rsid=281865118
|Orientation=minus
|Chromosome=13
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SACS
|position=23336372
|Gene_s=SACS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=13
|CLNACC=RCV000005848.2
|CLNALLE=1
|CLNDBN=Spastic ataxia Charlevoix-Saguenay type
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1255:C1849140:270550:98
|CLNHGVS=NC_000013.10:g.23910511G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1255; 604490.0002
|Disease=Spastic ataxia Charlevoix-Saguenay type
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=23910511
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865118
|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.
}}