Variant (rsID / SNP)
rs6313
rs6313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR2A. Location: chromosome 13, position 47,469,940. Clinical significance in the table: Benign.
Reference-table entries
HTR2ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:47469940
- Cytoband
- 13q14.2
- HGVS
- NM_000621.5(HTR2A):c.102= (p.Ser34=)
- Allele change
- Silent
Associated conditions / phenotypes
Schizophrenia, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.