{{Rsnum
|rsid=13418455
|Chromosome=2
|position=180212022
|Orientation=plus
|GMAF=0.264
|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 | 44.2 | 46.0 | 9.7
| HCB | 62.8 | 32.1 | 5.1
| JPT | 50.0 | 42.9 | 7.1
| YRI | 72.8 | 25.9 | 1.4
| ASW | 70.2 | 24.6 | 5.3
| CHB | 62.8 | 32.1 | 5.1
| CHD | 63.3 | 31.2 | 5.5
| GIH | 77.2 | 21.8 | 1.0
| LWK | 86.4 | 13.6 | 0.0
| MEX | 44.8 | 50.0 | 5.2
| MKK | 64.1 | 31.4 | 4.5
| TSI | 37.3 | 42.2 | 20.6
| 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=T
  |Pval=1E-6
  |OR=1.06
  |ORtxt=[1.04-1.09]
  |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}}