rs4987852
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4987852(A;A) |
| Make rs4987852(A;G) |
| Make rs4987852(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 18 |
| Position | 63126688 |
| Gene | BCL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4987852 |
| dbSNP (classic) | rs4987852 |
| ClinGen | rs4987852 |
| ebi | rs4987852 |
| HLI | rs4987852 |
| Exac | rs4987852 |
| Gnomad | rs4987852 |
| Varsome | rs4987852 |
| LitVar | rs4987852 |
| Map | rs4987852 |
| PheGenI | rs4987852 |
| Biobank | rs4987852 |
| 1000 genomes | rs4987852 |
| hgdp | rs4987852 |
| ensembl | rs4987852 |
| geneview | rs4987852 |
| scholar | rs4987852 |
| rs4987852 | |
| pharmgkb | rs4987852 |
| gwascentral | rs4987852 |
| openSNP | rs4987852 |
| 23andMe | rs4987852 |
| SNPshot | rs4987852 |
| SNPdbe | rs4987852 |
| MSV3d | rs4987852 |
| GWAS Ctlg | rs4987852 |
| GMAF | 0.02801 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23770605 |
| Trait | Chronic lymphocytic leukemia |
| Title | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. |
| Risk Allele | |
| P-val | 8E-11 |
| Odds Ratio | 1.41 [NR] |
[PMID 22037783] Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
