rs2456449
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2456449(A;A) |
| Make rs2456449(A;G) |
| Make rs2456449(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 127180736 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2456449 |
| dbSNP (classic) | rs2456449 |
| ClinGen | rs2456449 |
| ebi | rs2456449 |
| HLI | rs2456449 |
| Exac | rs2456449 |
| Gnomad | rs2456449 |
| Varsome | rs2456449 |
| LitVar | rs2456449 |
| Map | rs2456449 |
| PheGenI | rs2456449 |
| Biobank | rs2456449 |
| 1000 genomes | rs2456449 |
| hgdp | rs2456449 |
| ensembl | rs2456449 |
| geneview | rs2456449 |
| scholar | rs2456449 |
| rs2456449 | |
| pharmgkb | rs2456449 |
| gwascentral | rs2456449 |
| openSNP | rs2456449 |
| 23andMe | rs2456449 |
| SNPshot | rs2456449 |
| SNPdbe | rs2456449 |
| MSV3d | rs2456449 |
| GWAS Ctlg | rs2456449 |
| GMAF | 0.3228 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062064 ]
|
| Trait | Chronic lymphocytic leukemia |
| Title | Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk |
| Risk Allele | G |
| P-val | 8E-10 |
| Odds Ratio | 1.26 [1.17-1.35] |
[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis
