{{Rsnum
|rsid=159788
|Chromosome=20
|position=4371457
|Orientation=plus
|GMAF=0.1754
|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 | 0.9 | 18.8 | 80.4
| HCB | 8.1 | 40.7 | 51.1
| JPT | 2.7 | 39.3 | 58.0
| YRI | 4.8 | 31.0 | 64.1
| ASW | 7.0 | 22.8 | 70.2
| CHB | 8.1 | 40.7 | 51.1
| CHD | 15.0 | 40.2 | 44.9
| GIH | 2.0 | 29.3 | 68.7
| LWK | 2.8 | 25.2 | 72.0
| MEX | 0.0 | 24.6 | 75.4
| MKK | 1.9 | 22.6 | 75.5
| TSI | 1.0 | 24.5 | 74.5
| 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=G
  |Pval=7E-6
  |OR=1.01
  |ORtxt=[0.97-1.05]
  |OA=1
}}

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