rs11980379
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11980379(C;C) |
Make rs11980379(C;T) |
Make rs11980379(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 50402283 |
Gene | IKZF1 |
is a | snp |
is | mentioned by |
dbSNP | rs11980379 |
dbSNP (classic) | rs11980379 |
ClinGen | rs11980379 |
ebi | rs11980379 |
HLI | rs11980379 |
Exac | rs11980379 |
Gnomad | rs11980379 |
Varsome | rs11980379 |
LitVar | rs11980379 |
Map | rs11980379 |
PheGenI | rs11980379 |
Biobank | rs11980379 |
1000 genomes | rs11980379 |
hgdp | rs11980379 |
ensembl | rs11980379 |
geneview | rs11980379 |
scholar | rs11980379 |
rs11980379 | |
pharmgkb | rs11980379 |
gwascentral | rs11980379 |
openSNP | rs11980379 |
23andMe | rs11980379 |
SNPshot | rs11980379 |
SNPdbe | rs11980379 |
MSV3d | rs11980379 |
GWAS Ctlg | rs11980379 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23996088] |
Trait | Acute lymphoblastic leukemia (B-cell precursor) |
Title | Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. |
Risk Allele | |
P-val | 3E-33 |
Odds Ratio | NR NR |