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rs11979158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11979158(A;G)
Make rs11979158(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position55091656
GeneEGFR
is asnp
is mentioned by
dbSNPrs11979158
ebirs11979158
HLIrs11979158
Exacrs11979158
Varsomers11979158
Maprs11979158
PheGenIrs11979158
hapmaprs11979158
1000 genomesrs11979158
hgdprs11979158
ensemblrs11979158
gopubmedrs11979158
geneviewrs11979158
scholarrs11979158
googlers11979158
pharmgkbrs11979158
gwascentralrs11979158
openSNPrs11979158
23andMers11979158
23andMe allrs11979158
SNP Nexus

SNPshotrs11979158
SNPdbers11979158
MSV3drs11979158
GWAS Ctlgrs11979158
GMAF0.1593
Max Magnitude0
? (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 A
P-val 7E-8
Odds Ratio 1.2300 [1.15-1.35]

Associated with glioma risk.

[PMID 21825990] Genetic causes of glioma: new leads in the labyrinth.


[PMID 23236348OA-icon.png] EGFR Gene Variants Are Associated with Specific Somatic Aberrations in Glioma


[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