{{Rsnum
|rsid=11931532
|Gene=BST1
|Chromosome=4
|position=15724143
|Orientation=plus
|GMAF=0.2351
|Gene_s=BST1
|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 | 0.0 | 5.3 | 94.7
| HCB | 22.1 | 52.2 | 25.7
| JPT | 27.4 | 55.8 | 16.8
| YRI | 11.6 | 38.8 | 49.7
| ASW | 7.0 | 45.6 | 47.4
| CHB | 22.1 | 52.2 | 25.7
| CHD | 33.9 | 41.3 | 24.8
| GIH | 6.9 | 25.7 | 67.3
| LWK | 8.2 | 43.6 | 48.2
| MEX | 3.4 | 24.1 | 72.4
| MKK | 3.2 | 26.9 | 69.9
| TSI | 0.0 | 4.9 | 95.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=23026536
|Title=Lack of association between BST1 polymorphisms and sporadic Parkinson's disease in a Japanese population
}}

{{PMID Auto
|PMID=20413655
|Title=Genetics of neurodegenerative diseases: insights from high-throughput resequencing.
|OA=1
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}