{{Rsnum
|rsid=1015657
|Chromosome=17
|position=70882346
|Orientation=plus
|GMAF=0.3659
|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 | 15.0 | 51.3 | 33.6
| HCB | 81.8 | 16.8 | 1.5
| JPT | 85.0 | 15.0 | 0.0
| YRI | 45.6 | 39.5 | 15.0
| ASW | 37.5 | 41.1 | 21.4
| CHB | 81.8 | 16.8 | 1.5
| CHD | 80.7 | 17.4 | 1.8
| GIH | 31.7 | 46.5 | 21.8
| LWK | 45.5 | 41.8 | 12.7
| MEX | 43.1 | 41.4 | 15.5
| MKK | 42.9 | 46.2 | 10.9
| TSI | 30.4 | 44.1 | 25.5
| 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=0.000002
|OR=1.3200
|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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}