{{Rsnum
|rsid=281865119
|Orientation=minus
|Chromosome=13
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SACS
|position=23332969
|Gene_s=SACS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000032007.1
|CLNALLE=1
|CLNDBN=Spastic ataxia Charlevoix-Saguenay type
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1255:C1849140:270550:98
|CLNHGVS=NC_000013.10:g.23907108C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1255
|Disease=Spastic ataxia Charlevoix-Saguenay type
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=23907108
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865119
|GENEINFO=SACS:26278
|GENE_ID=26278
|GENE_NAME=SACS
}}{{PMID Auto
|PMID=20876471
|Title=Mutations in SACS cause atypical and late-onset forms of ARSACS.
}}