{{Rsnum
|rsid=241453
|Gene=TAP2
|Chromosome=6
|position=32828449
|Orientation=minus
|GMAF=0.2741
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TAP2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 55.8 | 35.4 | 8.8
| HCB | 38.0 | 44.5 | 17.5
| JPT | 39.8 | 47.8 | 12.4
| YRI | 83.0 | 16.3 | 0.7
| ASW | 68.4 | 29.8 | 1.8
| CHB | 38.0 | 44.5 | 17.5
| CHD | 47.7 | 35.8 | 16.5
| GIH | 29.7 | 52.5 | 17.8
| LWK | 69.1 | 23.6 | 7.3
| MEX | 50.0 | 39.7 | 10.3
| MKK | 43.6 | 45.5 | 10.9
| TSI | 54.9 | 40.2 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19387463
|Title=Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC
|OA=1
}}

{{PMID Auto
|PMID=22495925
|Title=Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables.
}}

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