{{Rsnum
|rsid=121434381
|Chromosome=9
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SETX
|position=132331123
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SETX
}}{{omim
|id=608465
|rsnum=121434381
|variant=0013
}}{{ClinVar
|rsid=121434381
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=135206510
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SETX:23064
|GENE_NAME=SETX
|GENE_ID=23064
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.135206510C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608465.0013
|CLNSIG=5
|CLNCUI=C1853761
|CLNDBN=Spinocerebellar ataxia autosomal recessive 1
|Disease=Spinocerebellar ataxia autosomal recessive 1
|CLNACC=RCV000002386.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1154:C1853761:606002:64753
}}