{{Rsnum
|rsid=9461045
|Gene=TDP2
|Chromosome=6
|position=24648833
|Orientation=plus
|GMAF=0.3255
|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 | 61.9 | 31.9 | 6.2
| HCB | 23.0 | 50.4 | 26.7
| JPT | 10.7 | 48.2 | 41.1
| YRI | 65.3 | 34.0 | 0.7
| ASW | 66.7 | 29.8 | 3.5
| CHB | 23.0 | 50.4 | 26.7
| CHD | 13.9 | 42.6 | 43.5
| GIH | 30.7 | 53.5 | 15.8
| LWK | 55.6 | 36.1 | 8.3
| MEX | 40.4 | 38.6 | 21.1
| MKK | 42.6 | 44.5 | 12.9
| TSI | 64.4 | 31.7 | 4.0
| HapMapRevision=28
}}[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000436 plos] linked to [[dyslexia]]

{{omim
|desc=DYSLEXIA, SUSCEPTIBILITY TO, 2; DYX2
|id=600202
|rsnum=9461045
}}

{{PMID|19325871|OA=1
}} A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

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