{{Rsnum
|rsid=7762160
|Gene=PDE10A
|Chromosome=6
|position=165601943
|Orientation=plus
|GMAF=0.3462
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PDE10A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 51.3 | 28.3
| HCB | 11.8 | 44.1 | 44.1
| JPT | 11.5 | 48.7 | 39.8
| YRI | 3.4 | 40.1 | 56.5
| ASW | 17.5 | 31.6 | 50.9
| CHB | 11.8 | 44.1 | 44.1
| CHD | 11.9 | 51.4 | 36.7
| GIH | 36.6 | 41.6 | 21.8
| LWK | 3.6 | 40.0 | 56.4
| MEX | 8.6 | 37.9 | 53.4
| MKK | 6.4 | 44.2 | 49.4
| TSI | 18.6 | 46.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (symptom count)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=0.000001
|OR=0.07
|ORtxt=[NR] unit increase
|OA=1
}}

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