Gene entry
HTR1B
5-hydroxytryptamine receptor 1B
- Chromosome
- 6
- Cytoband
- 6q14.1
- Variants (rsID)
- 6
HTR1B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q14.1). Its official name is “5-hydroxytryptamine receptor 1B”. The reference table lists 6 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs6296Not classifiedsynonymous_variantAlcohol Dependence|Gilles De La Tourette Syndrome|Mental Depression|Major Depressive Disorder|Depression|Attention Deficit-Hyperactivity Disorder|Obsessive-Compulsive Disorder|Epilepsy|Mood Disorder|Temporal Lobe Epilepsy|Scoliosis|Idiopathic Scoliosis|Scoliosis, Isolated 1|Generalized Anxiety Disorder|Migraine with or Without Aura 1|Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Fibromyalgia
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.