{{Rsnum
|rsid=1902341
|Gene=OSBPL10
|Chromosome=3
|position=31754078
|Orientation=minus
|GMAF=0.4619
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=OSBPL10
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 22.1 | 48.7 | 29.2
| HCB | 42.3 | 41.6 | 16.1
| JPT | 38.1 | 48.7 | 13.3
| YRI | 34.9 | 50.0 | 15.1
| ASW | 19.3 | 57.9 | 22.8
| CHB | 42.3 | 41.6 | 16.1
| CHD | 43.1 | 40.4 | 16.5
| GIH | 22.8 | 50.5 | 26.7
| LWK | 39.1 | 47.3 | 13.6
| MEX | 36.2 | 39.7 | 24.1
| MKK | 24.5 | 40.0 | 35.5
| TSI | 12.7 | 49.0 | 38.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20610895
|Trait=Peripheral artery disease
|Title=Identification of Evidence Suggestive of an Association with Peripheral Arterial Disease at the OSBPL10 Locus by Genome-Wide Investigation in the Japanese Population
|RiskAllele=G
|Pval=5E-7
|OR=1.31
|ORtxt=[1.18-1.46]
}}

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