{{Rsnum
|rsid=3806156
|Gene=BTNL2
|Chromosome=6
|position=32405921
|Orientation=plus
|GMAF=0.3714
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=BTNL2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 37.2 | 46.0 | 16.8
| HCB | 32.8 | 47.4 | 19.7
| JPT | 25.7 | 47.8 | 26.5
| YRI | 50.3 | 44.2 | 5.4
| ASW | 54.4 | 38.6 | 7.0
| CHB | 32.8 | 47.4 | 19.7
| CHD | 39.4 | 44.0 | 16.5
| GIH | 34.7 | 51.5 | 13.9
| LWK | 68.2 | 26.4 | 5.5
| MEX | 22.4 | 50.0 | 27.6
| MKK | 66.7 | 31.4 | 1.9
| TSI | 47.1 | 42.2 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20410501
|Trait=Vitiligo
|Title=Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
|RiskAllele=T
|Pval=7E-19
|OR=1.42
|ORtxt=[1.32-1.54]
|OA=1
}}

{{omim
|id=193200
|rsnum=3806156
}}

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

{{PMID Auto
|PMID=19458352
|Title=Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
|OA=1
}}

{{PMID Auto
|PMID=20017995
|Title=A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.
|OA=1
}}

{{PMID Auto
|PMID=20018063
|Title=Detecting significant single-nucleotide polymorphisms in a rheumatoid arthritis study using random forests.
|OA=1
}}

{{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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{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}}