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rs2252586

From SNPedia

Orientationminus
Stabilizedminus
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)
ReferenceGRCh38 38.1/142
Chromosome7
Position54911231
is asnp
is mentioned by
dbSNPrs2252586
ebirs2252586
HLIrs2252586
Exacrs2252586
Varsomers2252586
Maprs2252586
PheGenIrs2252586
hapmaprs2252586
1000 genomesrs2252586
hgdprs2252586
ensemblrs2252586
gopubmedrs2252586
geneviewrs2252586
scholarrs2252586
googlers2252586
pharmgkbrs2252586
gwascentralrs2252586
openSNPrs2252586
23andMers2252586
23andMe allrs2252586
SNP Nexus

SNPshotrs2252586
SNPdbers2252586
MSV3drs2252586
GWAS Ctlgrs2252586
GMAF0.2089
Max Magnitude1.4
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21531791OA-icon.png]
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 23161787OA-icon.png] 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