{{Rsnum
|rsid=16891867
|Gene=C1QTNF7
|Chromosome=4
|position=15395740
|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 | 92.9 | 7.1 | 0.0
| HCB | 69.3 | 28.5 | 2.2
| JPT | 60.2 | 36.3 | 3.5
| YRI | 63.9 | 30.6 | 5.4
| ASW | 57.9 | 36.8 | 5.3
| CHB | 69.3 | 28.5 | 2.2
| CHD | 73.4 | 23.9 | 2.8
| GIH | 91.1 | 8.9 | 0.0
| LWK | 54.6 | 39.8 | 5.6
| MEX | 63.8 | 34.5 | 1.7
| MKK | 66.0 | 33.3 | 0.6
| TSI | 92.2 | 7.8 | 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=3E-9
|OR=0.15
|ORtxt=[NR] unit increase
|OA=1
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}