{{Rsnum
|rsid=4236032
|Gene=KIAA0319
|Chromosome=6
|position=24606499
|Orientation=plus
|GMAF=0.05969
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KIAA0319
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 82.3 | 16.8 | 0.9
| HCB | 97.1 | 2.9 | 0.0
| JPT | 93.8 | 5.3 | 0.9
| YRI | 92.5 | 7.5 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 97.1 | 2.9 | 0.0
| CHD | 97.2 | 2.8 | 0.0
| GIH | 86.1 | 11.9 | 2.0
| LWK | 89.1 | 10.0 | 0.9
| MEX | 98.3 | 1.7 | 0.0
| MKK | 74.4 | 22.4 | 3.2
| TSI | 81.4 | 17.6 | 1.0
| HapMapRevision=28
}}Further evidence that the KIAA0319 gene confers susceptibility to developmental [[dyslexia]].{{PMID|17033633}}

{{PMID Auto
|PMID=15514892
|Title=A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
|OA=1
}}

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