{{Rsnum
|rsid=158856
|Gene=NEDD4L
|Chromosome=18
|position=58243291
|Orientation=plus
|GMAF=0.2851
|Gene_s=NEDD4L
|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 | 44.2 | 43.4 | 12.4
| HCB | 46.3 | 41.9 | 11.8
| JPT | 67.0 | 30.4 | 2.7
| YRI | 75.9 | 20.7 | 3.4
| ASW | 80.7 | 17.5 | 1.8
| CHB | 46.3 | 41.9 | 11.8
| CHD | 51.9 | 38.0 | 10.2
| GIH | 57.0 | 38.0 | 5.0
| LWK | 68.6 | 26.7 | 4.8
| MEX | 29.8 | 61.4 | 8.8
| MKK | 72.9 | 25.2 | 1.9
| TSI | 36.3 | 49.0 | 14.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22754043
  |Trait=Insomnia (caffeine-induced)
  |Title=A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.
  |RiskAllele=
  |Pval=7E-6
  |OR=1.41
  |ORtxt=[1.20-1.61]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}