{{Rsnum
|rsid=2015586
|Gene=SLC18A2
|Chromosome=10
|position=119021737
|Orientation=plus
|GMAF=0.438
|Gene_s=SLC18A2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 20.0 | 53.3 | 26.7
| JPT | 15.9 | 54.5 | 29.5
| YRI | 23.8 | 54.0 | 22.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 20.0 | 53.3 | 26.7
| 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=24018103
|Title=Association study of the vesicular monoamine transporter gene SLC18A2 with tardive dyskinesia
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}