{{Rsnum
|rsid=2125623
|Gene=OTUD7A
|Chromosome=15
|position=31537504
|Orientation=plus
|GMAF=0.3214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=OTUD7A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 48.7 | 41.6 | 9.7
| HCB | 45.3 | 43.8 | 10.9
| JPT | 56.6 | 36.3 | 7.1
| YRI | 33.1 | 50.3 | 16.6
| ASW | 38.2 | 49.1 | 12.7
| CHB | 45.3 | 43.8 | 10.9
| CHD | 44.0 | 45.0 | 11.0
| GIH | 69.3 | 27.7 | 3.0
| LWK | 36.7 | 52.3 | 11.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 44.2 | 41.0 | 14.7
| TSI | 49.0 | 42.2 | 8.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20400778
|Trait=Mortality among heart failure patients
|Title=Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium
|RiskAllele=C
|Pval=0.000001
|OR=1.23
|ORtxt=[0.99-1.54]
|OA=1
}}

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