{{Rsnum
|rsid=211105
|Gene=TPH1
|Chromosome=11
|position=18033757
|Orientation=plus
|GMAF=0.1607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=TPH1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 8.0 | 34.5 | 57.5
| HCB | 5.8 | 28.5 | 65.7
| JPT | 1.8 | 23.0 | 75.2
| YRI | 0.0 | 6.2 | 93.8
| ASW | 0.0 | 17.5 | 82.5
| CHB | 5.8 | 28.5 | 65.7
| CHD | 1.8 | 38.5 | 59.6
| GIH | 2.0 | 24.8 | 73.3
| LWK | 0.0 | 4.5 | 95.5
| MEX | 1.7 | 46.6 | 51.7
| MKK | 0.0 | 7.7 | 92.3
| TSI | 6.9 | 36.3 | 56.9
| HapMapRevision=28
}}[[rs211105]], [[rs1800532]] and [[rs7933505]] related to [[schizophrenia]]

{{PMID|15799788|OA=1
}} Polymorphism screening and haplotype analysis of the tryptophan hydroxylase gene (TPH1) and association with bipolar affective disorder in Taiwan.

{{PMID|20580984}} Tryptophan hydroxylase gene 1 (TPH1) variants associated with cerebrospinal fluid 5-hydroxyindole acetic acid and homovanillic acid concentrations in healthy volunteers.

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}