{{Rsnum
|rsid=7169523
|Chromosome=15
|position=31171175
|Orientation=plus
|GMAF=0.2897
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 35.4 | 62.8
| HCB | 45.3 | 44.5 | 10.2
| JPT | 39.8 | 46.0 | 14.2
| YRI | 0.0 | 6.8 | 93.2
| ASW | 0.0 | 12.3 | 87.7
| CHB | 45.3 | 44.5 | 10.2
| CHD | 51.4 | 42.2 | 6.4
| GIH | 6.9 | 29.7 | 63.4
| LWK | 0.0 | 9.1 | 90.9
| MEX | 1.7 | 22.4 | 75.9
| MKK | 3.2 | 14.7 | 82.1
| TSI | 4.0 | 27.7 | 68.3
| 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=G
  |Pval=2E-6
  |OR=1.40
  |ORtxt=[1.22-1.60]
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}