{{Rsnum
|rsid=12115114
|Chromosome=8
|position=63477322
|Orientation=plus
|GMAF=0.09826
|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 | 3.5 | 25.7 | 70.8
| HCB | 0.0 | 9.5 | 90.5
| JPT | 0.0 | 2.7 | 97.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 10.5 | 89.5
| CHB | 0.0 | 9.5 | 90.5
| CHD | 0.0 | 8.3 | 91.7
| GIH | 0.0 | 15.8 | 84.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 19.0 | 81.0
| MKK | 0.0 | 1.3 | 98.7
| TSI | 2.0 | 28.4 | 69.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=22194214
|Title=Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes
}}

{{PMID Auto
|PMID=20007504
|Title=Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.
|OA=1
}}

{{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}}