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