rs17239025
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17239025(C;C) |
| Make rs17239025(C;G) |
| Make rs17239025(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 30765768 |
| Gene | ALOX5AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17239025 |
| dbSNP (classic) | rs17239025 |
| ClinGen | rs17239025 |
| ebi | rs17239025 |
| HLI | rs17239025 |
| Exac | rs17239025 |
| Gnomad | rs17239025 |
| Varsome | rs17239025 |
| LitVar | rs17239025 |
| Map | rs17239025 |
| PheGenI | rs17239025 |
| Biobank | rs17239025 |
| 1000 genomes | rs17239025 |
| hgdp | rs17239025 |
| ensembl | rs17239025 |
| geneview | rs17239025 |
| scholar | rs17239025 |
| rs17239025 | |
| pharmgkb | rs17239025 |
| gwascentral | rs17239025 |
| openSNP | rs17239025 |
| 23andMe | rs17239025 |
| SNPshot | rs17239025 |
| SNPdbe | rs17239025 |
| MSV3d | rs17239025 |
| GWAS Ctlg | rs17239025 |
| GMAF | 0.04637 |
| Max Magnitude | 0 |
[PMID 23404351
] Genetic variation in the lipoxygenase pathway and risk of colorectal neoplasia
