rs1569175
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1569175(A;A) |
| Make rs1569175(A;G) |
| Make rs1569175(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 200157231 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1569175 |
| dbSNP (classic) | rs1569175 |
| ClinGen | rs1569175 |
| ebi | rs1569175 |
| HLI | rs1569175 |
| Exac | rs1569175 |
| Gnomad | rs1569175 |
| Varsome | rs1569175 |
| LitVar | rs1569175 |
| Map | rs1569175 |
| PheGenI | rs1569175 |
| Biobank | rs1569175 |
| 1000 genomes | rs1569175 |
| hgdp | rs1569175 |
| ensembl | rs1569175 |
| geneview | rs1569175 |
| scholar | rs1569175 |
| rs1569175 | |
| pharmgkb | rs1569175 |
| gwascentral | rs1569175 |
| openSNP | rs1569175 |
| 23andMe | rs1569175 |
| SNPshot | rs1569175 |
| SNPdbe | rs1569175 |
| MSV3d | rs1569175 |
| GWAS Ctlg | rs1569175 |
| GMAF | 0.1607 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | T |
| P-val | 9E-7 |
| Odds Ratio | 2.73 [1.52-4.93] |
