rs6958497
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs6958497(C;C) |
Make rs6958497(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 55094053 |
Gene | EGFR |
is a | snp |
is | mentioned by |
dbSNP | rs6958497 |
dbSNP (classic) | rs6958497 |
ClinGen | rs6958497 |
ebi | rs6958497 |
HLI | rs6958497 |
Exac | rs6958497 |
Gnomad | rs6958497 |
Varsome | rs6958497 |
LitVar | rs6958497 |
Map | rs6958497 |
PheGenI | rs6958497 |
Biobank | rs6958497 |
1000 genomes | rs6958497 |
hgdp | rs6958497 |
ensembl | rs6958497 |
geneview | rs6958497 |
scholar | rs6958497 |
rs6958497 | |
pharmgkb | rs6958497 |
gwascentral | rs6958497 |
openSNP | rs6958497 |
23andMe | rs6958497 |
SNPshot | rs6958497 |
SNPdbe | rs6958497 |
MSV3d | rs6958497 |
GWAS Ctlg | rs6958497 |
GMAF | 0.1272 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20400478] Polymorphisms in EGFR and VEGF contribute to non-small-cell lung cancer survival in a Chinese population
[PMID 19190167] A two-stage case-control study of EGFR polymorphisms and breast cancer risk.