{{Rsnum
|rsid=12606138
|Gene=NEDD4L
|Chromosome=18
|position=58326712
|Orientation=plus
|GMAF=0.1736
|Gene_s=NEDD4L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 60.2 | 38.1 | 1.8
| HCB | 83.9 | 15.3 | 0.7
| JPT | 81.4 | 18.6 | 0.0
| YRI | 61.2 | 34.0 | 4.8
| ASW | 66.7 | 28.1 | 5.3
| CHB | 83.9 | 15.3 | 0.7
| CHD | 81.7 | 17.4 | 0.9
| GIH | 84.2 | 14.9 | 1.0
| LWK | 65.5 | 30.9 | 3.6
| MEX | 77.6 | 22.4 | 0.0
| MKK | 60.9 | 35.3 | 3.8
| TSI | 77.5 | 18.6 | 3.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=24373531
|Title=Genetic risk variants for dyslexia on chromosome 18 in a German cohort
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}