rs1800532
| SNP: rs1800532 | |
|---|---|
| Name(s) | A218C |
| Gene | TPH1 |
| Chromosome | 11 |
| Region | Intron 7 |
| External databases | |
| Ensembl | Human SNPView |
| dbSNP | 1800532 |
| HapMap | 1800532 |
| SNPedia | 1800532 |
In genetics, rs1800532 (A218C) is a genetic variant. It is a single nucleotide polymorphism in the TPH1 gene and located in intron 7.
It has been examined in relation to personality traits.[1][2][3]
A779C is another SNP in same intron.
References[]
- ^ , , & (2003). "Allelic variants of the tryptophan hydroxylase (A218C) and serotonin 1B receptor (A-161T) and personality traits". Neuropsychobiology. 48 (2): 68–71. doi:10.1159/000072879. PMID 14504413. S2CID 42559772.CS1 maint: multiple names: authors list (link)
- ^ , , , Peter Singer, , , , & (July 2005). "The TPH intron 7 A218C polymorphism and TCI dimension scores in alcohol-dependent patients: hints to nonspecific psychopathology". Addictive Behaviors. 30 (6): 1135–43. doi:10.1016/j.addbeh.2004.11.002. PMID 15925123.CS1 maint: multiple names: authors list (link)
- ^ , , , , , & (March 2007). "No association between the TPH A218C polymorphism and personality traits in Japanese healthy subjects". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 31 (2): 395–398. doi:10.1016/j.pnpbp.2006.10.003. PMID 17116352. S2CID 30569509.CS1 maint: multiple names: authors list (link)
Categories:
- SNPs on chromosome 11