{{Rsnum
|rsid=9945428
|Gene=FBXO15
|Chromosome=18
|position=74121441
|Orientation=plus
|GMAF=0.4155
|Gene_s=FBXO15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 8.0 | 26.5 | 65.5
| HCB | 15.4 | 52.2 | 32.4
| JPT | 20.4 | 57.5 | 22.1
| YRI | 34.0 | 50.3 | 15.6
| ASW | 31.6 | 47.4 | 21.1
| CHB | 15.4 | 52.2 | 32.4
| CHD | 17.6 | 49.1 | 33.3
| GIH | 3.0 | 35.6 | 61.4
| LWK | 45.4 | 44.4 | 10.2
| MEX | 15.5 | 46.6 | 37.9
| MKK | 36.8 | 45.8 | 17.4
| TSI | 11.8 | 37.3 | 51.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=7E-9
  |OR=1.61
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}