{{Rsnum
|rsid=12302829
|Gene=FMR1NB
|Chromosome=12
|position=5031318
|Orientation=plus
|GMAF=0.0101
|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 | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 90.5 | 9.5 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 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=0.000008
|OR=0.35
|ORtxt=[NR] unit decrease
|OA=1
}}

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