rs16905439
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16905439(C;C) |
| Make rs16905439(C;T) |
| Make rs16905439(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 135976961 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16905439 |
| dbSNP (classic) | rs16905439 |
| ClinGen | rs16905439 |
| ebi | rs16905439 |
| HLI | rs16905439 |
| Exac | rs16905439 |
| Gnomad | rs16905439 |
| Varsome | rs16905439 |
| LitVar | rs16905439 |
| Map | rs16905439 |
| PheGenI | rs16905439 |
| Biobank | rs16905439 |
| 1000 genomes | rs16905439 |
| hgdp | rs16905439 |
| ensembl | rs16905439 |
| geneview | rs16905439 |
| scholar | rs16905439 |
| rs16905439 | |
| pharmgkb | rs16905439 |
| gwascentral | rs16905439 |
| openSNP | rs16905439 |
| 23andMe | rs16905439 |
| SNPshot | rs16905439 |
| SNPdbe | rs16905439 |
| MSV3d | rs16905439 |
| GWAS Ctlg | rs16905439 |
| GMAF | 0.1047 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [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. |
| Risk Allele | |
| P-val | 9E-6 |
| Odds Ratio | 3.33 [1.96-5.88] |
