Rs1799913
{{Infobox single nucleotide polymorphism
| rsid = 1799913
| name_1 = A779C
| gene = TPH1
| chromosome = 11
| region = Intron 7
| szgene_geneid = 111
| szgene_polyid = 586
}}
In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene.
It is located in intron 7.{{Cite journal
| author = D. A. Nielsen, G. L. Jenkins, K. M. Stefanisko, K. K. Jefferson & D. Goldman
| title = Sequence, splice site and population frequency distribution analyses of the polymorphic human tryptophan hydroxylase intron 7
| journal = Brain Research. Molecular Brain Research
| volume = 45
| issue = 1
| pages = 145–148
|date=April 1997
| pmid = 9105682
| doi = 10.1016/S0169-328X(96)00304-X
| url = https://zenodo.org/record/1259929
}}
The SNP association with schizophrenia has been examined in several studies, though as of 2007 with no definitive conclusion.{{Cite journal
| author = P. G. Sand
| title = Comments on the paper by D. Li and L. He: Meta-analysis shows association between the tryptophan hydroxylase (TPH) gene and schizophrenia
| journal = Human Genetics
| volume = 122
| issue = 3–4
|date=November 2007
| doi = 10.1007/s00439-007-0383-6
| pages = 409–411
| pmid = 17653577
| s2cid = 13181665
}}
One study has found that the SNP may be associated with heroin addiction.{{Cite journal
| author = David A. Nielsen, Sandra Barral, Dmitri Proudnikov, Scott Kellogg, Ann Ho, Jurg Ott & Mary Jeanne Kreek
| title = TPH2 and TPH1: association of variants and interactions with heroin addiction
| journal = Behavior Genetics
| volume = 38
| issue = 2
| pages = 133–50
|date=March 2008
| doi = 10.1007/s10519-007-9187-7
| pmid = 18181017
| s2cid = 2774846
}} Other study relate it to figural and numeric creativity.{{Cite journal
| author = Reuter M, Roth S, Holve K & Hennig J.
| title = Identification of first candidate genes for creativity: a pilot study.
| journal = Brain Res.
| year = 2006
| volume = 1069
| issue = 1
| pages = 190–197
| doi = 10.1016/j.brainres.2005.11.046
| pmid = 16403463
| s2cid = 25365017
}}
A218C (rs1800532) is another SNP in the same intron in the same gene.
References
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