{{Rsnum
|rsid=7799006
|Gene=FTSJ2
|Chromosome=7
|position=2238591
|Orientation=plus
|GMAF=0.3682
|Gene_s=FTSJ2
|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 | 43.8 | 43.8 | 12.5
| HCB | 24.1 | 52.6 | 23.4
| JPT | 35.7 | 51.8 | 12.5
| YRI | 49.7 | 44.2 | 6.1
| ASW | 54.4 | 38.6 | 7.0
| CHB | 24.1 | 52.6 | 23.4
| CHD | 24.8 | 46.8 | 28.4
| GIH | 32.7 | 55.4 | 11.9
| LWK | 55.5 | 37.3 | 7.3
| MEX | 31.0 | 56.9 | 12.1
| MKK | 63.5 | 34.0 | 2.6
| TSI | 44.1 | 43.1 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23453885
  |Trait=Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
  |Title=Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
  |RiskAllele=C
  |Pval=5E-6
  |OR=1.06
  |ORtxt=[1.03-1.08]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}