Human SNP ID | rs158856 |
---|---|
Human chromosome | chr18 |
Human SNP position | 58243291 |
Pig chromosome | chr1 |
Pig SNP position | 180140686 |
PubMed ID | 22754043 |
---|---|
Journal | Sleep |
Link | www.ncbi.nlm.nih.gov/pubmed/22754043 |
Study | A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. |
Disease/Trait | Insomnia (caffeine-induced) |
Initial sample | 2,402 European ancestry individuals from 1,470 families |
Replication sample | NA |
Region | 18q21.31 |
Chromosome id | chr18 |
Chromosome position | 58243291 |
Reported gene | NEDD4L |
Mapped gene | NEDD4L |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 23327 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs158856-? |
SNPs | rs158856 |
Merged | 0 |
SNP id current | 158856 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.66 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | 1.41 |
%95 Ci | [1.20-1.61] |
Platform | Illumina [2380486] (imputed) |
CNV | N |
Mapped trait | insomnia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004698 |
Study accession | GCST001586 |