{{Rsnum
|rsid=12871532
|Chromosome=13
|position=108016199
|Orientation=plus
|GMAF=0.4881
|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 | 21.2 | 52.2 | 26.5
| HCB | 52.6 | 40.1 | 7.3
| JPT | 31.0 | 56.6 | 12.4
| YRI | 6.8 | 32.7 | 60.5
| ASW | 10.5 | 45.6 | 43.9
| CHB | 52.6 | 40.1 | 7.3
| CHD | 47.2 | 43.5 | 9.3
| GIH | 29.7 | 55.4 | 14.9
| LWK | 6.4 | 28.2 | 65.5
| MEX | 27.6 | 51.7 | 20.7
| MKK | 5.8 | 40.4 | 53.8
| TSI | 19.6 | 40.2 | 40.2
| 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=T
  |Pval=1E-6
  |OR=1.06
  |ORtxt=[1.04-1.09]
  |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}}