rs11979158

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs11979158(A;G)

Make rs11979158(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

55091656

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs11979158
dbSNP (classic)	rs11979158
ClinGen	rs11979158
ebi	rs11979158
HLI	rs11979158
Exac	rs11979158
Gnomad	rs11979158
Varsome	rs11979158
LitVar	rs11979158
Map	rs11979158
PheGenI	rs11979158
Biobank	rs11979158
1000 genomes	rs11979158
hgdp	rs11979158
ensembl	rs11979158
geneview	rs11979158
scholar	rs11979158
google	rs11979158
pharmgkb	rs11979158
gwascentral	rs11979158
openSNP	rs11979158
23andMe	rs11979158
SNPshot	rs11979158
SNPdbe	rs11979158
MSV3d	rs11979158
GWAS Ctlg	rs11979158

GMAF

0.1593

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

GWAS snp
PMID	[PMID 21531791 ]
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 23236348 ] EGFR Gene Variants Are Associated with Specific Somatic Aberrations in Glioma

[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

[PMID 30152087 ] Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age.