{{Rsnum
|rsid=2076533
|Gene=BTNL2
|Chromosome=6
|position=32395750
|Orientation=minus
|GMAF=0.365
|Gene_s=BTNL2
|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 | 23.0 | 46.9 | 30.1
| HCB | 11.7 | 38.0 | 50.4
| JPT | 21.4 | 42.0 | 36.6
| YRI | 5.4 | 44.2 | 50.3
| ASW | 10.7 | 41.1 | 48.2
| CHB | 11.7 | 38.0 | 50.4
| CHD | 3.7 | 36.7 | 59.6
| GIH | 16.0 | 49.0 | 35.0
| LWK | 5.5 | 26.6 | 67.9
| MEX | 24.1 | 60.3 | 15.5
| MKK | 2.6 | 32.5 | 64.9
| TSI | 14.7 | 38.2 | 47.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=22991420
|Title=Genetic characterization and susceptibility for sarcoidosis in Japanese patients: risk factors of BTNL2 gene polymorphisms and HLA class II alleles
}}

{{PMID Auto
|PMID=17660530
|Title=Risk alleles for multiple sclerosis identified by a genomewide study.
}}

{{PMID Auto
|PMID=20018019
|Title=Two-stage joint selection method to identify candidate markers from genome-wide association studies.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}