{{Rsnum
|rsid=489332
|Chromosome=9
|position=75413430
|Orientation=plus
|GMAF=0.1758
|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 | 69.9 | 26.5 | 3.5
| HCB | 89.1 | 10.9 | 0.0
| JPT | 77.0 | 22.1 | 0.9
| YRI | 44.9 | 44.9 | 10.2
| ASW | 59.6 | 31.6 | 8.8
| CHB | 89.1 | 10.9 | 0.0
| CHD | 90.7 | 8.3 | 0.9
| GIH | 77.2 | 22.8 | 0.0
| LWK | 39.1 | 53.6 | 7.3
| MEX | 74.1 | 25.9 | 0.0
| MKK | 46.8 | 41.0 | 12.2
| TSI | 58.8 | 37.3 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23212062
  |Trait=Schizophrenia
  |Title=Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
  |RiskAllele=
  |Pval=6E-6
  |OR=.11
  |ORtxt=[NR] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}