{{Rsnum
|rsid=7620754
|Gene=DRD3
|Chromosome=3
|position=114229128
|Orientation=plus
|GMAF=0.2732
|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 | 8.0 | 42.5 | 49.6
| HCB | 10.9 | 49.6 | 39.4
| JPT | 15.0 | 37.2 | 47.8
| YRI | 9.5 | 33.3 | 57.1
| ASW | 5.3 | 38.6 | 56.1
| CHB | 10.9 | 49.6 | 39.4
| CHD | 10.1 | 49.5 | 40.4
| GIH | 6.9 | 44.6 | 48.5
| LWK | 10.0 | 42.7 | 47.3
| MEX | 8.6 | 48.3 | 43.1
| MKK | 16.7 | 46.2 | 37.2
| TSI | 5.9 | 39.2 | 54.9
| HapMapRevision=28
}}

{{PMID|19217756}} a haplotype containing [[rs3732782]], [[rs905568]], and [[rs7620754]] in the 5' region of [[DRD3]] was associated with Tardive dyskinesia diagnosis

{{PMID Auto
|PMID=19044451
|Title=Furnace enclosure
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}