rs6971925
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs6971925(C;T) |
Make rs6971925(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 14406292 |
Gene | DGKB |
is a | snp |
is | mentioned by |
dbSNP | rs6971925 |
dbSNP (classic) | rs6971925 |
ClinGen | rs6971925 |
ebi | rs6971925 |
HLI | rs6971925 |
Exac | rs6971925 |
Gnomad | rs6971925 |
Varsome | rs6971925 |
LitVar | rs6971925 |
Map | rs6971925 |
PheGenI | rs6971925 |
Biobank | rs6971925 |
1000 genomes | rs6971925 |
hgdp | rs6971925 |
ensembl | rs6971925 |
geneview | rs6971925 |
scholar | rs6971925 |
rs6971925 | |
pharmgkb | rs6971925 |
gwascentral | rs6971925 |
openSNP | rs6971925 |
23andMe | rs6971925 |
SNPshot | rs6971925 |
SNPdbe | rs6971925 |
MSV3d | rs6971925 |
GWAS Ctlg | rs6971925 |
GMAF | 0.04729 |
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 | 0.000003 |
Odds Ratio | 13.91 [2.72-70.92] |