{{Rsnum
|rsid=10770140
|Gene=TH
|Chromosome=11
|position=2172367
|Orientation=plus
|GMAF=0.3549
|Gene_s=MIR4686,TH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.0 | 50.9 | 29.1
| HCB | 2.4 | 14.6 | 82.9
| JPT | 0.0 | 16.7 | 83.3
| YRI | 29.4 | 41.2 | 29.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.4 | 14.6 | 82.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20571875
|Title=Human Tyrosine Hydroxylase Natural Allelic Variation: Influence on Autonomic Function and Hypertension
|OA=1
}}{{PMID Auto
|PMID=19604093
|Title=Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.
|OA=1
}}