{{Rsnum
|rsid=11838918
|Gene=LINC00331
|Chromosome=13
|position=78836439
|Orientation=plus
|GMAF=0.01607
|Gene_s=LINC00331
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.7 | 17.7 | 81.6
| ASW | 1.8 | 15.8 | 82.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 11.8 | 88.2
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.6 | 13.5 | 85.9
| TSI | 0.0 | 0.0 | 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=0.000003
|OR=2.26
|ORtxt=[1.61-3.18]
|OA=1
}}

{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}