rs10508343
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs10508343(A;A) |
Make rs10508343(A;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 8108750 |
is a | snp |
is | mentioned by |
dbSNP | rs10508343 |
dbSNP (classic) | rs10508343 |
ClinGen | rs10508343 |
ebi | rs10508343 |
HLI | rs10508343 |
Exac | rs10508343 |
Gnomad | rs10508343 |
Varsome | rs10508343 |
LitVar | rs10508343 |
Map | rs10508343 |
PheGenI | rs10508343 |
Biobank | rs10508343 |
1000 genomes | rs10508343 |
hgdp | rs10508343 |
ensembl | rs10508343 |
geneview | rs10508343 |
scholar | rs10508343 |
rs10508343 | |
pharmgkb | rs10508343 |
gwascentral | rs10508343 |
openSNP | rs10508343 |
23andMe | rs10508343 |
SNPshot | rs10508343 |
SNPdbe | rs10508343 |
MSV3d | rs10508343 |
GWAS Ctlg | rs10508343 |
GMAF | 0.0404 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 3.81 [1.40-10.40] |