{{Rsnum
|rsid=9296068
|Chromosome=6
|position=33020918
|Orientation=plus
|GMAF=0.4518
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 9.7 | 42.5 | 47.8
| HCB | 27.0 | 43.8 | 29.2
| JPT | 45.1 | 39.8 | 15.0
| YRI | 45.2 | 45.2 | 9.6
| ASW | 23.2 | 53.6 | 23.2
| CHB | 27.0 | 43.8 | 29.2
| CHD | 20.4 | 49.1 | 30.6
| GIH | 20.8 | 49.5 | 29.7
| LWK | 27.3 | 39.1 | 33.6
| MEX | 17.2 | 32.8 | 50.0
| MKK | 13.5 | 48.7 | 37.8
| TSI | 13.7 | 48.0 | 38.2
| HapMapRevision=28
}}{{PMID|18639552|OA=1
}}  rs9296068 significantly different (P = .018) in parent-to-child transmission between outcome groups. The minor allele of the SNP rs9296068 is significantly associated with liver transplantation rejection and with enhanced B-lymphocyte participation in rejection, likely because of a dysfunctional HLA-DOA gene product.

{{PMID Auto
|PMID=23991122
|Title=SNP Association Mapping across the Extended Major Histocompatibility Complex and Risk of B-Cell Precursor Acute Lymphoblastic Leukemia in Children
|OA=1
}}

{{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}}