{{Rsnum
|rsid=6719884
|Gene=AIRE
|Chromosome=2
|position=58809781
|Orientation=plus
|GMAF=0.449
|Gene_s=AIRE
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 15.0 | 54.0 | 31.0
| HCB | 30.7 | 46.7 | 22.6
| JPT | 36.3 | 45.1 | 18.6
| YRI | 17.0 | 44.9 | 38.1
| ASW | 14.0 | 49.1 | 36.8
| CHB | 30.7 | 46.7 | 22.6
| CHD | 33.9 | 50.5 | 15.6
| GIH | 11.9 | 44.6 | 43.6
| LWK | 16.4 | 44.5 | 39.1
| MEX | 22.4 | 48.3 | 29.3
| MKK | 17.3 | 46.8 | 35.9
| TSI | 24.5 | 36.3 | 39.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23055271
  |Trait=Myasthenia gravis
  |Title=Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
  |RiskAllele=A
  |Pval=3E-6
  |OR=1.35
  |ORtxt=[1.19-1.52]
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}