rs4947986
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4947986(A;A) |
Make rs4947986(A;G) |
Make rs4947986(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 55153962 |
Gene | EGFR |
is a | snp |
is | mentioned by |
dbSNP | rs4947986 |
dbSNP (classic) | rs4947986 |
ClinGen | rs4947986 |
ebi | rs4947986 |
HLI | rs4947986 |
Exac | rs4947986 |
Gnomad | rs4947986 |
Varsome | rs4947986 |
LitVar | rs4947986 |
Map | rs4947986 |
PheGenI | rs4947986 |
Biobank | rs4947986 |
1000 genomes | rs4947986 |
hgdp | rs4947986 |
ensembl | rs4947986 |
geneview | rs4947986 |
scholar | rs4947986 |
rs4947986 | |
pharmgkb | rs4947986 |
gwascentral | rs4947986 |
openSNP | rs4947986 |
23andMe | rs4947986 |
SNPshot | rs4947986 |
SNPdbe | rs4947986 |
MSV3d | rs4947986 |
GWAS Ctlg | rs4947986 |
GMAF | 0.332 |
Max Magnitude | 0 |
? | (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.