rs12762303
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12762303(C;C) |
| Make rs12762303(C;T) |
| Make rs12762303(T;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 10 |
| Position | 45373723 |
| Gene | ALOX5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12762303 |
| dbSNP (classic) | rs12762303 |
| ClinGen | rs12762303 |
| ebi | rs12762303 |
| HLI | rs12762303 |
| Exac | rs12762303 |
| Gnomad | rs12762303 |
| Varsome | rs12762303 |
| LitVar | rs12762303 |
| Map | rs12762303 |
| PheGenI | rs12762303 |
| Biobank | rs12762303 |
| 1000 genomes | rs12762303 |
| hgdp | rs12762303 |
| ensembl | rs12762303 |
| geneview | rs12762303 |
| scholar | rs12762303 |
| rs12762303 | |
| pharmgkb | rs12762303 |
| gwascentral | rs12762303 |
| openSNP | rs12762303 |
| 23andMe | rs12762303 |
| SNPshot | rs12762303 |
| SNPdbe | rs12762303 |
| MSV3d | rs12762303 |
| GWAS Ctlg | rs12762303 |
| GMAF | 0.1791 |
| Max Magnitude | 0 |
[PMID 18366677
] Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission.
[PMID 18369664] Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.
[PMID 30678701] Genetic variation in the leukotriene pathway is associated with myocardial infarction in the Chinese population.
