{{Rsnum
|rsid=10776612
|Gene=ARHGAP22
|Chromosome=10
|position=49735563
|Orientation=plus
|GMAF=0.4536
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.4 | 57.8 | 12.8
| HCB | 30.1 | 49.3 | 20.6
| JPT | 46.9 | 40.7 | 12.4
| YRI | 12.9 | 44.9 | 42.2
| ASW | 22.8 | 45.6 | 31.6
| CHB | 30.1 | 49.3 | 20.6
| CHD | 33.3 | 52.8 | 13.9
| GIH | 21.2 | 54.5 | 24.2
| LWK | 6.4 | 59.1 | 34.5
| MEX | 33.3 | 49.1 | 17.5
| MKK | 22.4 | 44.9 | 32.7
| TSI | 39.4 | 45.5 | 15.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (case status)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=0.000002
|OR=1.33
|ORtxt=[1.18-1.49]
|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}}