rs2228064
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs2228064(A;A) |
| Make rs2228064(A;G) |
| Reference | GRCh37.p5 37.3/135 |
| Chromosome | 10 |
| Position | 45382602 |
| Gene | ALOX5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228064 |
| dbSNP (classic) | rs2228064 |
| ClinGen | rs2228064 |
| ebi | rs2228064 |
| HLI | rs2228064 |
| Exac | rs2228064 |
| Gnomad | rs2228064 |
| Varsome | rs2228064 |
| LitVar | rs2228064 |
| Map | rs2228064 |
| PheGenI | rs2228064 |
| Biobank | rs2228064 |
| 1000 genomes | rs2228064 |
| hgdp | rs2228064 |
| ensembl | rs2228064 |
| geneview | rs2228064 |
| scholar | rs2228064 |
| rs2228064 | |
| pharmgkb | rs2228064 |
| gwascentral | rs2228064 |
| openSNP | rs2228064 |
| 23andMe | rs2228064 |
| SNPshot | rs2228064 |
| SNPdbe | rs2228064 |
| MSV3d | rs2228064 |
| GWAS Ctlg | rs2228064 |
| GMAF | 0.1019 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population
[PMID 18248681
] Prevalence of common disease-associated variants in Asian Indians.
[PMID 32027251] [Relationship between Polymorphism in ALOX5, ALOX5AP and Susceptibility to Myeloid Leukemia].
