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rs4947986

From SNPedia

Orientationplus
Stabilizedplus
Make rs4947986(A;A)
Make rs4947986(A;G)
Make rs4947986(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position55153962
GeneEGFR
is asnp
is mentioned by
dbSNPrs4947986
ebirs4947986
HLIrs4947986
Exacrs4947986
Varsomers4947986
Maprs4947986
PheGenIrs4947986
hapmaprs4947986
1000 genomesrs4947986
hgdprs4947986
ensemblrs4947986
gopubmedrs4947986
geneviewrs4947986
scholarrs4947986
googlers4947986
pharmgkbrs4947986
gwascentralrs4947986
openSNPrs4947986
23andMers4947986
23andMe allrs4947986
SNP Nexus

SNPshotrs4947986
SNPdbers4947986
MSV3drs4947986
GWAS Ctlgrs4947986
GMAF0.332
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20446891] A comprehensive study of the association between the EGFR and ERBB2 genes and glioma risk


[PMID 26906551] Pre-diagnostic serum levels of EGFR and ErbB2 and genetic glioma risk variants: a nested case-control study.