Rs1800532 Explained
| Rsid: | 1800532 |
| Name 1: | A218C |
| Region: | Intron 7 |
| Gene: | TPH1 |
| Chromosome: | 11 |
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.
Notes and References
- . Allelic variants of the tryptophan hydroxylase (A218C) and serotonin 1B receptor (A-161T) and personality traits . . 48 . 2 . 68–71 . 2003 . 10.1159/000072879 . 14504413. 42559772 .
- . The TPH intron 7 A218C polymorphism and TCI dimension scores in alcohol-dependent patients: hints to nonspecific psychopathology . . 30 . 6 . 1135–43 . July 2005 . 10.1016/j.addbeh.2004.11.002 . 15925123.
- . No association between the TPH A218C polymorphism and personality traits in Japanese healthy subjects . . 31 . 2 . 395–398 . March 2007 . 10.1016/j.pnpbp.2006.10.003 . 17116352. 30569509 .
