{{Rsnum
|rsid=1480380
|Chromosome=6
|position=32945469
|Orientation=plus
|GMAF=0.0955
|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 | 86.7 | 13.3 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 51.7 | 40.8 | 7.5
| ASW | 71.9 | 26.3 | 1.8
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 55.5 | 39.1 | 5.5
| MEX | 89.7 | 10.3 | 0.0
| MKK | 80.1 | 19.2 | 0.6
| TSI | 87.3 | 11.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23453885
  |Trait=Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
  |Title=Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
  |RiskAllele=C
  |Pval=6E-7
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}