{{Rsnum
|rsid=1861050
|Gene=CC2D2A
|Chromosome=4
|position=15480736
|Orientation=plus
|GMAF=0.1107
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CC2D2A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 92.9 | 7.1 | 0.0
| HCB | 74.5 | 22.6 | 2.9
| JPT | 61.9 | 35.4 | 2.7
| YRI | 78.9 | 20.4 | 0.7
| ASW | 77.2 | 22.8 | 0.0
| CHB | 74.5 | 22.6 | 2.9
| CHD | 78.0 | 20.2 | 1.8
| GIH | 91.1 | 8.9 | 0.0
| LWK | 82.7 | 15.5 | 1.8
| MEX | 68.4 | 31.6 | 0.0
| MKK | 67.9 | 30.1 | 1.9
| TSI | 92.2 | 7.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (case status)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=0.000008
|OR=1.63
|ORtxt=[1.31-2.01]
|OA=1
}}

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