Gene entry
TGM6
transglutaminase 6
- Chromosome
- 20
- Cytoband
- 20p13
- Variants (rsID)
- 28
TGM6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p13). Its official name is “transglutaminase 6”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs116904482Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs142679146Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs147494925Benignsingle nucleotide variant
- rs148376598Benignsingle nucleotide variant
- rs183670042Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs2076405Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs74338361Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs79724097Benignsingle nucleotide variantSpinocerebellar ataxia type 35
- rs201964784Uncertain significancesingle nucleotide variantSpinocerebellar ataxia type 35
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.