{{Rsnum
|rsid=761100
|Gene=KIAA0319
|Chromosome=6
|position=24632414
|Orientation=minus
|GMAF=0.3173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=KIAA0319
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 25.9 | 57.1 | 17.0
| HCB | 74.8 | 24.4 | 0.7
| JPT | 82.7 | 16.4 | 0.9
| YRI | 50.3 | 38.8 | 10.9
| ASW | 50.9 | 43.9 | 5.3
| CHB | 74.8 | 24.4 | 0.7
| CHD | 81.3 | 17.8 | 0.9
| GIH | 34.7 | 52.5 | 12.9
| LWK | 52.7 | 41.8 | 5.5
| MEX | 51.7 | 43.1 | 5.2
| MKK | 47.4 | 39.6 | 13.0
| TSI | 28.4 | 48.0 | 23.5
| HapMapRevision=28
}}The more common allele of [[rs761100]] has been linked to increased risk for developmental [[dyslexia]] in a study of ~300 British families. While odds ratios were not reported, the significance was reported as p=0.02.{{PMID|17033633}}

{{PMID|19997522|OA=1
}} Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.

[[Developmental Dyslexia]]

{{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}}