Gene entry
HTT
huntingtin
- Chromosome
- 4
- Cytoband
- 4p16.3
- Variants (rsID)
- 26
HTT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4p16.3). Its official name is “huntingtin”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs34315806Benignsingle nucleotide variantLopes-Maciel-Rodan syndrome
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.