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rs121913428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913428(C;C)
Make rs121913428(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position55174015
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913428
ebirs121913428
HLIrs121913428
Exacrs121913428
Varsomers121913428
Maprs121913428
PheGenIrs121913428
hapmaprs121913428
1000 genomesrs121913428
hgdprs121913428
ensemblrs121913428
gopubmedrs121913428
geneviewrs121913428
scholarrs121913428
googlers121913428
pharmgkbrs121913428
gwascentralrs121913428
openSNPrs121913428
23andMers121913428
23andMe allrs121913428
SNP Nexus

SNPshotrs121913428
SNPdbers121913428
MSV3drs121913428
GWAS Ctlgrs121913428
Max Magnitude0
ClinVar
Risk rs121913428(A,C;A,C)
Alt rs121913428(A,C;A,C)
Reference rs121913428(G;G)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55241708G>C
CLNSRC ClinVar
CLNACC RCV000038381.2,