rs2388082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2388082(C;C) |
Make rs2388082(C;G) |
Make rs2388082(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 29387195 |
Gene | MTUS2 |
is a | snp |
is | mentioned by |
dbSNP | rs2388082 |
dbSNP (classic) | rs2388082 |
ClinGen | rs2388082 |
ebi | rs2388082 |
HLI | rs2388082 |
Exac | rs2388082 |
Gnomad | rs2388082 |
Varsome | rs2388082 |
LitVar | rs2388082 |
Map | rs2388082 |
PheGenI | rs2388082 |
Biobank | rs2388082 |
1000 genomes | rs2388082 |
hgdp | rs2388082 |
ensembl | rs2388082 |
geneview | rs2388082 |
scholar | rs2388082 |
rs2388082 | |
pharmgkb | rs2388082 |
gwascentral | rs2388082 |
openSNP | rs2388082 |
23andMe | rs2388082 |
SNPshot | rs2388082 |
SNPdbe | rs2388082 |
MSV3d | rs2388082 |
GWAS Ctlg | rs2388082 |
GMAF | 0.1198 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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 | 4E-6 |
Odds Ratio | 1.69 [1.35-2.13] |