Variant (rsID / SNP)
rs6296
rs6296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR1B. Location: chromosome 6, position 78,172,260. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 6:78172260
- HGVS
- NM_000863.3,c.861G>C,p.Val287Val
- Allele change
- Synonymous_V287V
Associated conditions / phenotypes
Alcohol 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
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.