Gene entry
TOR1A
torsin family 1 member A
- Chromosome
- 9
- Cytoband
- 9q34.11
- Variants (rsID)
- 7
TOR1A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.11). Its official name is “torsin family 1 member A”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs1801968Benignsingle nucleotide variantDystonia 1, torsion, modifier of|Early-onset generalized limb-onset dystonia|Dystonic disorder
- rs199535970Conflicting interpretationssingle nucleotide variantEarly-onset generalized limb-onset dystonia|Dystonic disorder
- rs267607134Conflicting interpretationssingle nucleotide variantDystonia 1, torsion, late-onset|Early-onset generalized limb-onset dystonia|Dystonic disorder
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.