rs17222919
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17222919(G;G) |
| Make rs17222919(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 30734192 |
| Gene | ALOX5AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17222919 |
| dbSNP (classic) | rs17222919 |
| ClinGen | rs17222919 |
| ebi | rs17222919 |
| HLI | rs17222919 |
| Exac | rs17222919 |
| Gnomad | rs17222919 |
| Varsome | rs17222919 |
| LitVar | rs17222919 |
| Map | rs17222919 |
| PheGenI | rs17222919 |
| Biobank | rs17222919 |
| 1000 genomes | rs17222919 |
| hgdp | rs17222919 |
| ensembl | rs17222919 |
| geneview | rs17222919 |
| scholar | rs17222919 |
| rs17222919 | |
| pharmgkb | rs17222919 |
| gwascentral | rs17222919 |
| openSNP | rs17222919 |
| 23andMe | rs17222919 |
| SNPshot | rs17222919 |
| SNPdbe | rs17222919 |
| MSV3d | rs17222919 |
| GWAS Ctlg | rs17222919 |
| GMAF | 0.1607 |
| Max Magnitude | 0 |
[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population
[PMID 20592751
] Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.
[PMID 25815512] A Promoter Polymorphism (rs17222919, -1316T/G) of ALOX5AP Gene Is Associated with Decreased Risk of Ischemic Stroke in Two Independent Chinese Populations
[PMID 27416969] Genetic Variants in the Transcriptional Regulatory Region of the ALOX5AP gene and Susceptibility to Ischemic Stroke in Chinese Populations.
