Variant (rsID / SNP)
rs17116138
rs17116138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR3B. Location: chromosome 11, position 113,803,666. The table records no clinical significance for this variant.
Reference-table entries
HTR3BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:113803666
- HGVS
- NM_006028.5,c.547G>A,p.Val183Ile
- Allele change
- Missense_V183I
Associated conditions / phenotypes
Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.