{{Rsnum
|rsid=10947261
|Gene=BTNL2
|Chromosome=6
|position=32405455
|Orientation=plus
|GMAF=0.1644
|Gene_s=BTNL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 88.5 | 11.5 | 0.0
| HCB | 51.1 | 40.9 | 8.0
| JPT | 34.5 | 46.9 | 18.6
| YRI | 74.1 | 23.1 | 2.7
| ASW | 86.0 | 12.3 | 1.8
| CHB | 51.1 | 40.9 | 8.0
| CHD | 59.6 | 33.9 | 6.4
| GIH | 70.3 | 26.7 | 3.0
| LWK | 86.2 | 11.9 | 1.8
| MEX | 63.8 | 32.8 | 3.4
| MKK | 86.5 | 13.5 | 0.0
| TSI | 80.4 | 18.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23850713
  |Trait=Crohn's disease
  |Title=Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
  |RiskAllele=T
  |Pval=3E-12
  |OR=1.36
  |ORtxt=[1.25-1.49]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}