{{Rsnum
|rsid=6750486
|Chromosome=2
|position=35301852
|Orientation=plus
|GMAF=0.1313
|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 | 92.0 | 7.1 | 0.9
| HCB | 75.9 | 23.4 | 0.7
| JPT | 77.0 | 23.0 | 0.0
| YRI | 43.5 | 40.8 | 15.6
| ASW | 54.4 | 40.4 | 5.3
| CHB | 75.9 | 23.4 | 0.7
| CHD | 80.7 | 18.3 | 0.9
| GIH | 81.2 | 18.8 | 0.0
| LWK | 35.5 | 53.6 | 10.9
| MEX | 89.7 | 10.3 | 0.0
| MKK | 48.1 | 39.7 | 12.2
| TSI | 85.3 | 14.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (symptom count)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=0.000006
|OR=0.10
|ORtxt=[NR] unit increase
|OA=1
}}

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