{{Rsnum
|rsid=16831128
|Chromosome=2
|position=132386819
|Orientation=plus
|GMAF=0.1974
|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 | 71.7 | 24.8 | 3.5
| HCB | 66.4 | 29.9 | 3.6
| JPT | 58.4 | 37.2 | 4.4
| YRI | 78.2 | 21.1 | 0.7
| ASW | 71.9 | 24.6 | 3.5
| CHB | 66.4 | 29.9 | 3.6
| CHD | 74.3 | 22.9 | 2.8
| GIH | 40.6 | 45.5 | 13.9
| LWK | 78.2 | 20.9 | 0.9
| MEX | 48.3 | 37.9 | 13.8
| MKK | 72.4 | 25.0 | 2.6
| TSI | 59.8 | 32.4 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (case status)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=4E-7
|OR=1.45
|ORtxt=[1.26-1.67]
|OA=1
}}

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