{{Rsnum
|rsid=10947262
|Gene=BTNL2
|Chromosome=6
|position=32405535
|Orientation=plus
|GMAF=0.1703
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=BTNL2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 88.5 | 11.5 | 0.0
| HCB | 51.1 | 40.9 | 8.0
| JPT | 33.9 | 47.3 | 18.8
| YRI | 73.5 | 23.8 | 2.7
| ASW | 78.9 | 19.3 | 1.8
| CHB | 51.1 | 40.9 | 8.0
| CHD | 59.6 | 33.9 | 6.4
| GIH | 70.3 | 26.7 | 3.0
| LWK | 77.3 | 20.0 | 2.7
| MEX | 63.8 | 32.8 | 3.4
| MKK | 85.3 | 14.7 | 0.0
| TSI | 80.4 | 18.6 | 1.0
| HapMapRevision=28
}}

[[rs10947262]](C) was found to be associated with increased risk for [[osteoarthritis]] among Japanese and Europeans, with an odds ratio of 1.32 (CI: 1.19-1.46, combined p = 6.73×10e-8). This SNP is also in linkage disequilibrium with [[rs7775228]], which was found to be associated in Japanese with [[osteoarthritis]].{{PMID|20305777|OA=1
}}

{{PMID Auto GWAS
|PMID=20305777
|Trait=Knee osteoarthritis
|Title=New Sequence Variants in HLA Class II/III Region Associated with Susceptibility to Knee Osteoarthritis Identified by Genome-Wide Association Study
|RiskAllele=T
|Pval=5E-9
|OR=1.31
|ORtxt=[1.20-1.44]
|OA=1
}}

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