Human SNP ID | rs2065779 |
---|---|
Human chromosome | chr10 |
Human SNP position | 111118043 |
Pig chromosome | chr14 |
Pig SNP position | 132440465 |
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 | 10q25.2 |
Chromosome id | chr10 |
Chromosome position | 111118043 |
Reported gene | RP11-479A21.1 |
Mapped gene | ADRA2A - LOC105378484 |
Upstream gene id | 150 |
Downstream gene id | 105378484 |
SNP gene ids | |
Upstream gene distance | 37136 |
Downstream gene distance | 282238 |
SNP risk allele | rs2065779-? |
SNPs | rs2065779 |
Merged | 0 |
SNP id current | 2065779 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.93 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 1.82 |
%95 Ci | [1.41-2.33] |
Platform | Illumina [2380486] (imputed) |
CNV | N |
Mapped trait | insomnia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004698 |
Study accession | GCST001586 |