rs35229355
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs35229355(C;T) |
Make rs35229355(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 155608667 |
is a | snp |
is | mentioned by |
dbSNP | rs35229355 |
dbSNP (classic) | rs35229355 |
ClinGen | rs35229355 |
ebi | rs35229355 |
HLI | rs35229355 |
Exac | rs35229355 |
Gnomad | rs35229355 |
Varsome | rs35229355 |
LitVar | rs35229355 |
Map | rs35229355 |
PheGenI | rs35229355 |
Biobank | rs35229355 |
1000 genomes | rs35229355 |
hgdp | rs35229355 |
ensembl | rs35229355 |
geneview | rs35229355 |
scholar | rs35229355 |
rs35229355 | |
pharmgkb | rs35229355 |
gwascentral | rs35229355 |
openSNP | rs35229355 |
23andMe | rs35229355 |
SNPshot | rs35229355 |
SNPdbe | rs35229355 |
MSV3d | rs35229355 |
GWAS Ctlg | rs35229355 |
GMAF | 0.1396 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 0.000005 |
Odds Ratio | 7.24 [2.46-21.30] |