rs17007695
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17007695(C;C) |
| Make rs17007695(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 141788570 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17007695 |
| dbSNP (classic) | rs17007695 |
| ClinGen | rs17007695 |
| ebi | rs17007695 |
| HLI | rs17007695 |
| Exac | rs17007695 |
| Gnomad | rs17007695 |
| Varsome | rs17007695 |
| LitVar | rs17007695 |
| Map | rs17007695 |
| PheGenI | rs17007695 |
| Biobank | rs17007695 |
| 1000 genomes | rs17007695 |
| hgdp | rs17007695 |
| ensembl | rs17007695 |
| geneview | rs17007695 |
| scholar | rs17007695 |
| rs17007695 | |
| pharmgkb | rs17007695 |
| gwascentral | rs17007695 |
| openSNP | rs17007695 |
| 23andMe | rs17007695 |
| SNPshot | rs17007695 |
| SNPdbe | rs17007695 |
| MSV3d | rs17007695 |
| GWAS Ctlg | rs17007695 |
| GMAF | 0.1809 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19176441 ]
|
| Trait | Treatment response for acute lymphoblastic leukemia |
| Title | Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia |
| Risk Allele | C |
| P-val | 9E-7 |
| Odds Ratio | 2.67 [1.53-4.68] |
