{{Rsnum
|rsid=281865120
|Orientation=minus
|Chromosome=13
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SACS
|position=23331716
|Gene_s=SACS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=13
|CLNACC=RCV000032008.1
|CLNALLE=1
|CLNDBN=Spastic ataxia Charlevoix-Saguenay type
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1255:C1849140:270550:98
|CLNHGVS=NC_000013.10:g.23905855G>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1255
|Disease=Spastic ataxia Charlevoix-Saguenay type
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=23905855
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865120
|GENEINFO=SACS:26278
|GENE_ID=26278
|GENE_NAME=SACS
}}{{PMID Auto
|PMID=18465152
|Title=ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
|OA=1
}}