{{Rsnum
|rsid=11162922
|Chromosome=1
|position=80106373
|Orientation=plus
|GMAF=0.1938
|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 | 86.7 | 13.3 | 0.0
| HCB | 56.2 | 38.7 | 5.1
| JPT | 53.1 | 38.9 | 8.0
| YRI | 51.4 | 42.5 | 6.2
| ASW | 52.6 | 40.4 | 7.0
| CHB | 56.2 | 38.7 | 5.1
| CHD | 45.0 | 48.6 | 6.4
| GIH | 69.3 | 26.7 | 4.0
| LWK | 42.7 | 50.9 | 6.4
| MEX | 79.3 | 20.7 | 0.0
| MKK | 38.5 | 49.4 | 12.2
| TSI | 80.2 | 18.8 | 1.0
| HapMapRevision=28
}}
[[rs11162922]] has been reported in a large study to be associated with [[rheumatoid arthritis]].

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.27 (CI 0.41-4.01), and for homozygotes, 2.00 (CI 0.64-6.20). {{PMID|17554300|OA=1
}}

{{PMID Auto
|PMID=18794857
|Title=Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.
|OA=1
}}

{{PMID Auto
|PMID=20017963
|Title=Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.
|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}}