{{Rsnum
|rsid=10770141
|Gene=TH
|Chromosome=11
|position=2172610
|Orientation=plus
|GMAF=0.3604
|Gene_s=MIR4686,TH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 17.7 | 46.9 | 35.4
| HCB | 0.7 | 13.9 | 85.4
| JPT | 0.0 | 13.3 | 86.7
| YRI | 29.9 | 52.4 | 17.7
| ASW | 38.6 | 42.1 | 19.3
| CHB | 0.7 | 13.9 | 85.4
| CHD | 1.8 | 11.0 | 87.2
| GIH | 1.0 | 42.6 | 56.4
| LWK | 49.1 | 40.9 | 10.0
| MEX | 19.0 | 44.8 | 36.2
| MKK | 25.0 | 46.8 | 28.2
| TSI | 8.8 | 52.9 | 38.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=19958792
|Title=Association study between a functional polymorphism of tyrosine hydroxylase gene promoter and personality traits in healthy subjects
}}

{{PMID Auto
|PMID=20571875
|Title=Human Tyrosine Hydroxylase Natural Allelic Variation: Influence on Autonomic Function and Hypertension
|OA=1
}}

{{PMID Auto
|PMID=17717598
|Title=Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
|OA=1
}}

{{PMID Auto
|PMID=18180394
|Title=Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.
|OA=1
}}

{{PMID Auto
|PMID=23246742
|Title=Association of monoamine-synthesizing genes with the depression tendency and personality in chronic fatigue syndrome patients.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}