{{Rsnum
|rsid=363371
|Chromosome=10
|position=118986396
|Orientation=plus
|GMAF=0.2695
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 9.8 | 27.7 | 62.5
| HCB | 33.3 | 44.4 | 22.2
| JPT | 31.1 | 51.1 | 17.8
| YRI | 0.0 | 27.4 | 72.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 33.3 | 44.4 | 22.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 11.1 | 52.5 | 36.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.8 | 28.6 | 69.6
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{omim
|desc=SOLUTE CARRIER FAMILY 18 (VESICULAR MONOAMINE), MEMBER 2; SLC18A2
|id=193001
|rsnum=363371
}}

{{PMID Auto
|PMID=23369548
|Title=Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson's disease.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}