{{Rsnum
|rsid=12351590
|Chromosome=9
|position=12108916
|Orientation=plus
|GMAF=0.2475
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 91.2 | 7.1 | 1.8
| HCB | 23.1 | 55.2 | 21.6
| JPT | 32.7 | 45.5 | 21.8
| YRI | 68.5 | 28.8 | 2.7
| ASW | 63.2 | 33.3 | 3.5
| CHB | 23.1 | 55.2 | 21.6
| CHD | 23.8 | 53.3 | 22.9
| GIH | 68.0 | 30.0 | 2.0
| LWK | 54.5 | 39.1 | 6.4
| MEX | 43.9 | 36.8 | 19.3
| MKK | 67.7 | 26.5 | 5.8
| TSI | 84.3 | 15.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23738518
  |Trait=Reading and spelling
  |Title=A genome-wide association study for reading and language abilities in two population cohorts.
  |RiskAllele=
  |Pval=3E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=20525348
|Title=Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.
|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}}