rs6125048
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs6125048(G;T) |
Make rs6125048(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 47579861 |
Gene | NCOA3 |
is a | snp |
is | mentioned by |
dbSNP | rs6125048 |
dbSNP (classic) | rs6125048 |
ClinGen | rs6125048 |
ebi | rs6125048 |
HLI | rs6125048 |
Exac | rs6125048 |
Gnomad | rs6125048 |
Varsome | rs6125048 |
LitVar | rs6125048 |
Map | rs6125048 |
PheGenI | rs6125048 |
Biobank | rs6125048 |
1000 genomes | rs6125048 |
hgdp | rs6125048 |
ensembl | rs6125048 |
geneview | rs6125048 |
scholar | rs6125048 |
rs6125048 | |
pharmgkb | rs6125048 |
gwascentral | rs6125048 |
openSNP | rs6125048 |
23andMe | rs6125048 |
SNPshot | rs6125048 |
SNPdbe | rs6125048 |
MSV3d | rs6125048 |
GWAS Ctlg | rs6125048 |
GMAF | 0.152 |
Max Magnitude | 0 |
? | (G;G) (G;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 | 0.000002 |
Odds Ratio | 2.73 [1.08-6.88] |