{{Rsnum
|rsid=17693963
|Chromosome=6
|position=27742386
|Orientation=plus
|GMAF=0.04729
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 85.8 | 12.4 | 1.8
| HCB | 97.8 | 2.2 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 99.0 | 1.0 | 0.0
| LWK | 85.5 | 14.5 | 0.0
| MEX | 89.7 | 10.3 | 0.0
| MKK | 73.5 | 23.2 | 3.2
| TSI | 87.3 | 12.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22688191
|Trait=None
|Title=Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
|RiskAllele=
|Pval=3E-11
|OR=1.2400
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=19571809
|Title=Common variants on chromosome 6p22.1 are associated with schizophrenia.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=24166486
  |Trait=Schizophrenia, schizoaffective disorder or bipolar disorder
  |Title=GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.
  |RiskAllele=
  |Pval=2E-9
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=24280982
  |Trait=Schizophrenia or bipolar disorder
  |Title=Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
  |RiskAllele=
  |Pval=3E-11
  |OR=NR
  |ORtxt=NR
  }}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}