rs10828317
From SNPedia
| Merged into | rs2230469 |
| Orientation | minus |
| Stabilized | minus |
| Make rs10828317(A;A) |
| Make rs10828317(A;G) |
| Make rs10828317(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 22550699 |
| Gene | PIP4K2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10828317 |
| dbSNP (classic) | rs10828317 |
| ClinGen | rs10828317 |
| ebi | rs10828317 |
| HLI | rs10828317 |
| Exac | rs10828317 |
| Gnomad | rs10828317 |
| Varsome | rs10828317 |
| LitVar | rs10828317 |
| Map | rs10828317 |
| PheGenI | rs10828317 |
| Biobank | rs10828317 |
| 1000 genomes | rs10828317 |
| hgdp | rs10828317 |
| ensembl | rs10828317 |
| geneview | rs10828317 |
| scholar | rs10828317 |
| rs10828317 | |
| pharmgkb | rs10828317 |
| gwascentral | rs10828317 |
| openSNP | rs10828317 |
| 23andMe | rs10828317 |
| SNPshot | rs10828317 |
| SNPdbe | rs10828317 |
| MSV3d | rs10828317 |
| GWAS Ctlg | rs10828317 |
| Status | Merged into rs2230469 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23996088] |
| Trait | Acute lymphoblastic leukemia (B-cell precursor) |
| Title | Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. |
| Risk Allele | T |
| P-val | 2E-9 |
| Odds Ratio | 1.23 [1.15-1.32] |
