rs7115578
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7115578(A;A) |
Make rs7115578(A;G) |
Make rs7115578(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 96266936 |
Gene | MAML2 |
is a | snp |
is | mentioned by |
dbSNP | rs7115578 |
dbSNP (classic) | rs7115578 |
ClinGen | rs7115578 |
ebi | rs7115578 |
HLI | rs7115578 |
Exac | rs7115578 |
Gnomad | rs7115578 |
Varsome | rs7115578 |
LitVar | rs7115578 |
Map | rs7115578 |
PheGenI | rs7115578 |
Biobank | rs7115578 |
1000 genomes | rs7115578 |
hgdp | rs7115578 |
ensembl | rs7115578 |
geneview | rs7115578 |
scholar | rs7115578 |
rs7115578 | |
pharmgkb | rs7115578 |
gwascentral | rs7115578 |
openSNP | rs7115578 |
23andMe | rs7115578 |
SNPshot | rs7115578 |
SNPdbe | rs7115578 |
MSV3d | rs7115578 |
GWAS Ctlg | rs7115578 |
GMAF | 0.4265 |
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 | 0.000008 |
Odds Ratio | 1.86 [1.23-2.79] |