Variant (rsID / SNP)
rs1176713
rs1176713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR3A. Location: chromosome 11, position 113,860,425. The table records no clinical significance for this variant.
Reference-table entries
HTR3ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:113860425
- HGVS
- NM_213621.4,c.1473A>G,p.Leu491Leu
- Allele change
- Synonymous_L497L
Associated conditions / phenotypes
Alcohol Use Disorder|Major Affective Disorder 8|Schizophrenia|Major Affective Disorder 9|Constipation|Bipolar Disorder|Alcohol Dependence|Juvenile Rheumatoid Arthritis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.