{{Rsnum
|rsid=305217
|Gene=PKN2
|Chromosome=1
|position=88754789
|Orientation=minus
|GMAF=0.09229
|Gene_s=PKN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 90.8 | 9.2 | 0.0
| HCB | 71.1 | 26.7 | 2.2
| JPT | 88.6 | 11.4 | 0.0
| YRI | 63.6 | 32.9 | 3.5
| ASW | 78.6 | 19.6 | 1.8
| CHB | 71.1 | 26.7 | 2.2
| CHD | 73.3 | 23.8 | 2.9
| GIH | 94.9 | 5.1 | 0.0
| LWK | 64.2 | 33.0 | 2.8
| MEX | 0.0 | 0.0 | 0.0
| MKK | 66.9 | 29.2 | 3.9
| TSI | 0.0 | 0.0 | 0.0
| 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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}