{{Rsnum
|rsid=4538475
|Chromosome=4
|position=15736314
|Orientation=plus
|GMAF=0.3127
|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 | 69.9 | 29.2 | 0.9
| HCB | 23.5 | 52.2 | 24.3
| JPT | 15.9 | 47.8 | 36.3
| YRI | 42.2 | 44.9 | 12.9
| ASW | 45.6 | 47.4 | 7.0
| CHB | 23.5 | 52.2 | 24.3
| CHD | 19.3 | 44.0 | 36.7
| GIH | 58.4 | 33.7 | 7.9
| LWK | 60.0 | 32.7 | 7.3
| MEX | 46.6 | 44.8 | 8.6
| MKK | 30.1 | 46.8 | 23.1
| TSI | 75.5 | 22.5 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915576
|Trait=Parkinson's disease
|Title=Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
|RiskAllele=G
|Pval=3E-9
|OR=1.24
|ORtxt=[1.16-1.34]
}}

{{omim
|id=168600
|rsnum=4538475
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4538475
|overall_frequency_n=37
|overall_frequency_d=126
|overall_frequency=0.293651
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=30
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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