Variant (rsID / SNP)
rs1176744
rs1176744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR3B. Location: chromosome 11, position 113,803,028. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 11:113803028
- HGVS
- NM_006028.5,c.386A>C,p.Tyr129Ser
- Allele change
- Missense_Y129S
Associated conditions / phenotypes
Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Alcohol Dependence|Major Affective Disorder 5|Major Affective Disorder 1|Major Affective Disorder 6|Heroin Dependence|Drug Dependence|Generalized Anxiety Disorder|Schizophrenia|Obsessive-Compulsive Disorder|Bulimia Nervosa|Anorexia Nervosa|Juvenile Rheumatoid Arthritis|Arthritis|Eating Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.