{{Rsnum
|rsid=121434380
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SETX
|position=132296907
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SETX
}}{{omim
|id=608465
|rsnum=121434380
|variant=0012
}}{{ClinVar
|rsid=121434380
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=135172294
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SETX:23064
|GENE_NAME=SETX
|GENE_ID=23064
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.135172294G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608465.0012
|CLNSIG=5
|CLNCUI=C1853761
|CLNDBN=Spinocerebellar ataxia autosomal recessive 1
|Disease=Spinocerebellar ataxia autosomal recessive 1
|CLNACC=RCV000002385.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1154:C1853761:606002:64753
}}