rs546784
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs546784(A;A) |
Make rs546784(A;G) |
Make rs546784(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 66296783 |
Gene | PDE4B |
is a | snp |
is | mentioned by |
dbSNP | rs546784 |
dbSNP (classic) | rs546784 |
ClinGen | rs546784 |
ebi | rs546784 |
HLI | rs546784 |
Exac | rs546784 |
Gnomad | rs546784 |
Varsome | rs546784 |
LitVar | rs546784 |
Map | rs546784 |
PheGenI | rs546784 |
Biobank | rs546784 |
1000 genomes | rs546784 |
hgdp | rs546784 |
ensembl | rs546784 |
geneview | rs546784 |
scholar | rs546784 |
rs546784 | |
pharmgkb | rs546784 |
gwascentral | rs546784 |
openSNP | rs546784 |
23andMe | rs546784 |
SNPshot | rs546784 |
SNPdbe | rs546784 |
MSV3d | rs546784 |
GWAS Ctlg | rs546784 |
GMAF | 0.3365 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23007406] |
Trait | Acute lymphoblastic leukemia (childhood) |
Title | Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. |
Risk Allele | A |
P-val | 9E-6 |
Odds Ratio | 1.40 [1.20-1.62] |