{{Rsnum
|rsid=7164569
|Gene=OTUD7A
|Chromosome=15
|position=31501727
|Orientation=plus
|GMAF=0.3508
|Gene_s=OTUD7A
|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 | 35.4 | 51.3 | 13.3
| HCB | 59.9 | 34.3 | 5.8
| JPT | 58.4 | 35.4 | 6.2
| YRI | 27.9 | 42.9 | 29.3
| ASW | 26.3 | 49.1 | 24.6
| CHB | 59.9 | 34.3 | 5.8
| CHD | 57.4 | 36.1 | 6.5
| GIH | 60.4 | 34.7 | 5.0
| LWK | 30.9 | 50.9 | 18.2
| MEX | 25.9 | 55.2 | 19.0
| MKK | 41.7 | 46.8 | 11.5
| TSI | 39.2 | 52.0 | 8.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23650146
  |Trait=Venous thromboembolism
  |Title=A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
  |RiskAllele=A
  |Pval=3E-6
  |OR=1.15
  |ORtxt=[1.09-1.23]
  }}

{{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}}