{{Rsnum
|rsid=10250997
|Chromosome=7
|position=136461788
|Orientation=plus
|GMAF=0.09871
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 15.0 | 84.1
| HCB | 0.0 | 2.9 | 97.1
| JPT | 0.0 | 4.4 | 95.6
| YRI | 6.8 | 44.9 | 48.3
| ASW | 5.3 | 40.4 | 54.4
| CHB | 0.0 | 2.9 | 97.1
| CHD | 0.0 | 1.8 | 98.2
| GIH | 1.0 | 21.8 | 77.2
| LWK | 10.0 | 25.5 | 64.5
| MEX | 0.0 | 13.8 | 86.2
| MKK | 7.1 | 22.4 | 70.5
| TSI | 2.0 | 21.6 | 76.5
| 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=8E-6
  |OR=1.03
  |ORtxt=[0.99-1.07]
  |OA=1
}}

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