rs17885289
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs17885289(A;A) |
| Make rs17885289(A;G) |
| Make rs17885289(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 44386212 |
| Gene | CXCL12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17885289 |
| dbSNP (classic) | rs17885289 |
| ClinGen | rs17885289 |
| ebi | rs17885289 |
| HLI | rs17885289 |
| Exac | rs17885289 |
| Gnomad | rs17885289 |
| Varsome | rs17885289 |
| LitVar | rs17885289 |
| Map | rs17885289 |
| PheGenI | rs17885289 |
| Biobank | rs17885289 |
| 1000 genomes | rs17885289 |
| hgdp | rs17885289 |
| ensembl | rs17885289 |
| geneview | rs17885289 |
| scholar | rs17885289 |
| rs17885289 | |
| pharmgkb | rs17885289 |
| gwascentral | rs17885289 |
| openSNP | rs17885289 |
| 23andMe | rs17885289 |
| SNPshot | rs17885289 |
| SNPdbe | rs17885289 |
| MSV3d | rs17885289 |
| GWAS Ctlg | rs17885289 |
| GMAF | 0.2071 |
| Max Magnitude | 0 |
[PMID 19788587
] Genetic variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study
