{{Rsnum
|rsid=2242944
|Chromosome=21
|position=39093252
|Orientation=plus
|GMAF=0.4729
|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 | 16.2 | 45.9 | 37.8
| HCB | 15.9 | 54.5 | 29.5
| JPT | 11.4 | 43.2 | 45.5
| YRI | 68.7 | 29.9 | 1.4
| ASW | 51.8 | 37.5 | 10.7
| CHB | 15.9 | 54.5 | 29.5
| CHD | 12.3 | 52.8 | 34.9
| GIH | 16.8 | 43.6 | 39.6
| LWK | 48.2 | 38.2 | 13.6
| MEX | 18.5 | 51.9 | 29.6
| MKK | 35.3 | 55.1 | 9.6
| TSI | 17.8 | 49.5 | 32.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062062
|Trait=Ankylosing spondylitis
|Title=Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
|RiskAllele=A
|Pval=8E-20
|OR=1.39
|ORtxt=[1.28-1.49]
|OA=1
}}

23andMe reports that the GG genotype at [[rs2242944]] is associated with 1.4x higher odds of [[ankylosing spondylitis]], and the AA genotype is associated with 0.7x lower odds. {{PMID|20062062|OA=1
}} 

{{omim
|id=106300
|rsnum=2242944
}}

{{PMID|20810504}} Association of the intergenic single-nucleotide polymorphism rs10865331 (2p15) with ankylosing spondylitis in a Spanish population.

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