{{Rsnum
|rsid=12443954
|Chromosome=16
|position=89675088
|Orientation=plus
|GMAF=0.4247
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 59.3 | 34.5 | 6.2
| HCB | 5.2 | 32.6 | 62.2
| JPT | 7.2 | 37.8 | 55.0
| YRI | 43.4 | 42.8 | 13.8
| ASW | 47.4 | 47.4 | 5.3
| CHB | 5.2 | 32.6 | 62.2
| CHD | 2.9 | 20.0 | 77.1
| GIH | 23.0 | 55.0 | 22.0
| LWK | 32.7 | 50.9 | 16.4
| MEX | 29.3 | 55.2 | 15.5
| MKK | 50.0 | 39.3 | 10.7
| TSI | 63.7 | 33.3 | 2.9
| 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=A
  |Pval=1E-6
  |OR=1.08
  |ORtxt=[1.04-1.11]
  |OA=1
}}

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