{{Rsnum
|rsid=80358235
|Chromosome=9
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GTTCACCAAGTTAGATTA)
|geno3=(GTTCACCAAGTTAGATTA;GTTCACCAAGTTAGATTA)
|Gene=TOR1A
|position=129813988
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TOR1A
}}{{omim
|id=605204
|rsnum=80358235
|variant=0002
}}{{ClinVar
|rsid=80358235
|Reversed=1
|FwdREF=GTTCACCAAGTTAGATTA
|FwdALT=
|REF=ATAATCTAACTTGGTGAAC
|ALT=A
|RSPOS=132576266
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050168000000000002110200
|GENEINFO=TOR1A:1861
|GENE_NAME=TOR1A
|GENE_ID=1861
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.132576267_132576284del18
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1492; 605204.0002
|CLNSIG=5
|CLNCUI=C1851945
|CLNDBN=Dystonia, early-onset atypical, with myoclonic features; Dystonia 1
|Disease=Dystonia; Dystonia 1
|CLNACC=RCV000005489.1; RCV000020124.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1492:C1851945:128100:256
}}{{PMID Auto
|PMID=11523564
|Title=Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism.
}}

{{PMID Auto
|PMID=12391338
|Title=Inherited myoclonus-dystonia: how many causative genes and clinical phenotypes?
}}

{{PMID Auto
|PMID=12391355
|Title=Clinical findings of a myoclonus-dystonia family with two distinct mutations.
}}

{{PMID Auto
|PMID=12402271
|Title=Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations.
}}