Rs17483466
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17483466 |
| PheGenI | rs17483466 |
| nextbio | rs17483466 |
| hapmap | rs17483466 |
| 1000 genomes | rs17483466 |
| hgdp | rs17483466 |
| ensembl | rs17483466 |
| gopubmed | rs17483466 |
| geneview | rs17483466 |
| scholar | rs17483466 |
| rs17483466 | |
| pharmgkb | rs17483466 |
| gwascentral | rs17483466 |
| openSNP | rs17483466 |
| 23andMe | rs17483466 |
| 23andMe all | rs17483466 |
| SNP Nexus | |
| SNPshot | rs17483466 |
| SNPdbe | rs17483466 |
| MSV3d | rs17483466 |
| Gene | ACOXL |
| Chromosome | 2 |
| Orientation | plus |
| GMAF | 0.1186 |
| Position | 111797458 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs17483466(A;A) |
| Make rs17483466(A;G) |
| Make rs17483466(G;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
- rs17483466 G 1.39
| GWAS | |
|---|---|
| SNP | rs17483466 |
| PubMedID | [PMID 18758461] |
| Condition | Chronic lymphocytic leukemia |
| Gene | ACOXL,BCL2L11 |
| Risk Allele | G |
| pValue | 2.00E-010 |
| OR | 1.39 |
| 95% CI | 1.25-1.53 |
[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis
[PMID 20731705] Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.
| GWAS snp | |
|---|---|
| PMID | [PMID 22700719] |
| Trait | |
| Title | Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. |
| Risk Allele | |
| P-val | 5E-9 |
| Odds Ratio | 1.4300 None |
| GET Evidence | |
|---|---|
| rs17483466 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.103175 |
| summary | |
