{{Rsnum
|rsid=4964469
|Gene=LOC100287944
|Chromosome=12
|position=106556209
|Orientation=plus
|GMAF=0.4513
|Gene_s=RPL23P10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 21.2 | 40.7 | 38.1
| HCB | 12.6 | 51.1 | 36.3
| JPT | 18.8 | 35.7 | 45.5
| YRI | 39.3 | 48.3 | 12.4
| ASW | 36.8 | 50.9 | 12.3
| CHB | 12.6 | 51.1 | 36.3
| CHD | 21.5 | 46.7 | 31.8
| GIH | 11.9 | 55.4 | 32.7
| LWK | 48.1 | 40.7 | 11.1
| MEX | 5.2 | 43.1 | 51.7
| MKK | 36.5 | 46.8 | 16.7
| TSI | 13.7 | 46.1 | 40.2
| 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=2E-7
|OR=1.1600
|ORtxt=[1.09-1.22]
}}

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