{{Rsnum
|rsid=2359536
|Chromosome=10
|position=20899608
|Orientation=plus
|GMAF=0.2433
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 15.9 | 45.1 | 38.9
| HCB | 0.7 | 12.7 | 86.6
| JPT | 0.0 | 10.7 | 89.3
| YRI | 10.9 | 29.9 | 59.2
| ASW | 10.5 | 31.6 | 57.9
| CHB | 0.7 | 12.7 | 86.6
| CHD | 0.0 | 16.5 | 83.5
| GIH | 14.9 | 44.6 | 40.6
| LWK | 7.3 | 40.9 | 51.8
| MEX | 1.7 | 43.1 | 55.2
| MKK | 11.5 | 46.2 | 42.3
| TSI | 15.7 | 52.0 | 32.4
| 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=C
|Pval=0.000002
|OR=1.84
|ORtxt=[1.43-2.37]
}}

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