{{Rsnum
|rsid=121434378
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SETX
|position=132283403
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SETX
}}{{omim
|id=608465
|rsnum=121434378
|variant=0008
}}{{ClinVar
|rsid=121434378
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=135158790
|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.135158790C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608465.0008
|CLNSIG=5
|CLNCUI=C1865409
|CLNDBN=Amyotrophic lateral sclerosis type 4
|Disease=Amyotrophic lateral sclerosis type 4
|CLNACC=RCV000002381.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:C1865409:602433:357043
}}