{{Rsnum
|rsid=1861046
|Gene=C1QTNF7
|Chromosome=4
|position=15396282
|Orientation=plus
|GMAF=0.1478
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=C1QTNF7
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 7.1 | 92.9
| HCB | 2.2 | 28.5 | 69.3
| JPT | 3.5 | 36.3 | 60.2
| YRI | 5.4 | 30.6 | 63.9
| ASW | 5.3 | 38.6 | 56.1
| CHB | 2.2 | 28.5 | 69.3
| CHD | 2.8 | 23.9 | 73.4
| GIH | 0.0 | 8.9 | 91.1
| LWK | 4.5 | 40.9 | 54.5
| MEX | 1.7 | 34.5 | 63.8
| MKK | 1.3 | 32.1 | 66.7
| TSI | 0.0 | 7.8 | 92.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20585324
|Trait=Conduct disorder (case status)
|Title=Genome-wide association study of conduct disorder symptomatology
|RiskAllele=
|Pval=6E-8
|OR=1.65
|ORtxt=[1.38-1.98]
|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}}