{{Rsnum
|rsid=1783925
|Gene=PKNOX2
|Chromosome=11
|position=125434113
|Orientation=minus
|GMAF=0.2989
|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 | 9.8 | 39.3 | 50.9
| HCB | 8.8 | 45.3 | 46.0
| JPT | 16.8 | 56.6 | 26.5
| YRI | 0.0 | 18.4 | 81.6
| ASW | 0.0 | 33.3 | 66.7
| CHB | 8.8 | 45.3 | 46.0
| CHD | 10.3 | 48.6 | 41.1
| GIH | 5.0 | 31.7 | 63.4
| LWK | 1.8 | 8.2 | 90.0
| MEX | 24.1 | 48.3 | 27.6
| MKK | 1.3 | 22.6 | 76.1
| TSI | 13.7 | 37.3 | 49.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22648509
|Trait=None
|Title=PKNOX2 is Associated with Formal Thought Disorder in Schizophrenia: a Meta-Analysis of Two Genome-wide Association Studies.
|RiskAllele=
|Pval=4E-7
|OR=1.3900
|ORtxt=None
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}