{{Rsnum
|rsid=1256531
|Gene=PTBP1P
|Chromosome=14
|position=65281041
|Orientation=plus
|GMAF=0.2466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 87.6 | 11.5 | 0.9
| HCB | 63.5 | 35.8 | 0.7
| JPT | 59.3 | 32.7 | 8.0
| YRI | 10.9 | 50.3 | 38.8
| ASW | 22.8 | 52.6 | 24.6
| CHB | 63.5 | 35.8 | 0.7
| CHD | 64.2 | 34.9 | 0.9
| GIH | 67.3 | 29.7 | 3.0
| LWK | 13.1 | 51.4 | 35.5
| MEX | 82.8 | 17.2 | 0.0
| MKK | 19.2 | 50.0 | 30.8
| TSI | 81.4 | 18.6 | 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=0.000004
|OR=0.09
|ORtxt=[NR] unit increase
|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}}