rs267759
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs267759(A;A) |
Make rs267759(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 36137518 |
Gene | LMBRD2 |
is a | snp |
is | mentioned by |
dbSNP | rs267759 |
dbSNP (classic) | rs267759 |
ClinGen | rs267759 |
ebi | rs267759 |
HLI | rs267759 |
Exac | rs267759 |
Gnomad | rs267759 |
Varsome | rs267759 |
LitVar | rs267759 |
Map | rs267759 |
PheGenI | rs267759 |
Biobank | rs267759 |
1000 genomes | rs267759 |
hgdp | rs267759 |
ensembl | rs267759 |
geneview | rs267759 |
scholar | rs267759 |
rs267759 | |
pharmgkb | rs267759 |
gwascentral | rs267759 |
openSNP | rs267759 |
23andMe | rs267759 |
SNPshot | rs267759 |
SNPdbe | rs267759 |
MSV3d | rs267759 |
GWAS Ctlg | rs267759 |
GMAF | 0.1267 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19176441] |
Trait | Treatment response for acute lymphoblastic leukemia |
Title | Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia |
Risk Allele | A |
P-val | 0.000007 |
Odds Ratio | 3.23 [1.52-6.87] |