{{Rsnum
|rsid=11224899
|Chromosome=11
|position=97088525
|Orientation=plus
|GMAF=0.09917
|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 | 0.0 | 6.2 | 93.8
| HCB | 3.0 | 32.6 | 64.4
| JPT | 2.7 | 32.1 | 65.2
| YRI | 3.4 | 20.0 | 76.6
| ASW | 0.0 | 22.8 | 77.2
| CHB | 3.0 | 32.6 | 64.4
| CHD | 2.8 | 44.0 | 53.2
| GIH | 1.0 | 7.9 | 91.1
| LWK | 0.0 | 22.7 | 77.3
| MEX | 0.0 | 7.0 | 93.0
| MKK | 2.6 | 25.3 | 72.1
| TSI | 1.0 | 10.8 | 88.2
| 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=T
|Pval=0.000002
|OR=1.8989
|ORtxt=None
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}