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rs6958497

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6958497(C;C)
Make rs6958497(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position55094053
GeneEGFR
is asnp
is mentioned by
dbSNPrs6958497
ebirs6958497
HLIrs6958497
Exacrs6958497
Varsomers6958497
Maprs6958497
PheGenIrs6958497
hapmaprs6958497
1000 genomesrs6958497
hgdprs6958497
ensemblrs6958497
gopubmedrs6958497
geneviewrs6958497
scholarrs6958497
googlers6958497
pharmgkbrs6958497
gwascentralrs6958497
openSNPrs6958497
23andMers6958497
23andMe allrs6958497
SNP Nexus

SNPshotrs6958497
SNPdbers6958497
MSV3drs6958497
GWAS Ctlgrs6958497
GMAF0.1272
Max Magnitude0
? (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 19190167OA-icon.png] A two-stage case-control study of EGFR polymorphisms and breast cancer risk.