{{Rsnum
|rsid=34174194
|Chromosome=2
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=INO80B-WBP1
|position=74458316
|Gene_s=INO80B,INO80B-WBP1,WBP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 2.7 | 31.9 | 65.5
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 14.0 | 86.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 5.9 | 93.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.6 | 4.5 | 94.9
| TSI | 2.0 | 24.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=25143393
|Title=Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia
}}

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