rs2252586
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.4 | 1.4x higher risk for glioma development |
(A;G) | 1.2 | 1.2x higher risk for glioma development |
Make rs2252586(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 54911231 |
is a | snp |
is | mentioned by |
dbSNP | rs2252586 |
dbSNP (classic) | rs2252586 |
ClinGen | rs2252586 |
ebi | rs2252586 |
HLI | rs2252586 |
Exac | rs2252586 |
Gnomad | rs2252586 |
Varsome | rs2252586 |
LitVar | rs2252586 |
Map | rs2252586 |
PheGenI | rs2252586 |
Biobank | rs2252586 |
1000 genomes | rs2252586 |
hgdp | rs2252586 |
ensembl | rs2252586 |
geneview | rs2252586 |
scholar | rs2252586 |
rs2252586 | |
pharmgkb | rs2252586 |
gwascentral | rs2252586 |
openSNP | rs2252586 |
23andMe | rs2252586 |
SNPshot | rs2252586 |
SNPdbe | rs2252586 |
MSV3d | rs2252586 |
GWAS Ctlg | rs2252586 |
GMAF | 0.2089 |
Max Magnitude | 1.4 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21531791] |
Trait | |
Title | Chromosome 7p11.2 (EGFR) variation influences glioma risk. |
Risk Allele | T |
P-val | 8E-8 |
Odds Ratio | 1.1800 [1.11-1.25] |
Associated with glioma risk.
[PMID 21825990] Genetic causes of glioma: new leads in the labyrinth.
[PMID 23161787] Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies
[PMID 26243184] An Updated and Comprehensive Meta-Analysis of Association Between Seven Hot Loci Polymorphisms from Eight GWAS and Glioma Risk