Rs5789
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5789 |
| PheGenI | rs5789 |
| nextbio | rs5789 |
| hapmap | rs5789 |
| 1000 genomes | rs5789 |
| hgdp | rs5789 |
| ensembl | rs5789 |
| gopubmed | rs5789 |
| geneview | rs5789 |
| scholar | rs5789 |
| rs5789 | |
| pharmgkb | rs5789 |
| gwascentral | rs5789 |
| openSNP | rs5789 |
| 23andMe | rs5789 |
| 23andMe all | rs5789 |
| SNP Nexus | |
| SNPshot | rs5789 |
| SNPdbe | rs5789 |
| MSV3d | rs5789 |
| Gene | PTGS1 |
| Chromosome | 9 |
| Orientation | plus |
| GMAF | 0.0179 |
| Position | 125143973 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs5789(A;A) |
| Make rs5789(A;C) |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
[PMID 20214591] Pharmacogenomics in aspirin intolerance
[PMID 17301694] Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1).
[PMID 17495879] Cyclooxygenase polymorphisms and risk of cardiovascular events: the Atherosclerosis Risk in Communities (ARIC) study.
[PMID 21097517] Neurovascular coupling in the human visual cortex is modulated by cyclooxygenase-1 (COX-1) gene variant.
