{{Rsnum
|rsid=4698412
|Chromosome=4
|position=15735725
|Orientation=plus
|GMAF=0.405
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BST1
|Gene_s=BST1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 29.2 | 47.8 | 23.0
| HCB | 15.3 | 51.1 | 33.6
| JPT | 13.3 | 48.7 | 38.1
| YRI | 2.0 | 12.2 | 85.7
| ASW | 1.8 | 36.8 | 61.4
| CHB | 15.3 | 51.1 | 33.6
| CHD | 11.9 | 46.8 | 41.3
| GIH | 27.7 | 50.5 | 21.8
| LWK | 0.0 | 17.3 | 82.7
| MEX | 24.1 | 53.4 | 22.4
| MKK | 2.6 | 30.1 | 67.3
| TSI | 36.3 | 44.1 | 19.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21084426
|Trait=None
|Title=Genome-wide association study confirms BST1 and suggests a locus on 12q24 as risk loci for Parkinson's disease in the European population
|RiskAllele=A
|Pval=0.000002
|OR=1.1400
|ORtxt=[1.08-1.20]
}}
{{omim
|id=168600
|rsnum=4698412
}}

{{PMID Auto GWAS
|PMID=22451204
|Trait=None
|Title=Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|RiskAllele=
|Pval=3E-7
|OR=1.1400
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=19915575
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|OA=1
}}

{{PMID Auto
|PMID=21268244
|Title=Association of GWAS loci with PD in China.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}