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rs121913467

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913467(A;A)
Make rs121913467(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174730
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913467
dbSNP (old)rs121913467
ClinGenrs121913467
ebirs121913467
HLIrs121913467
Exacrs121913467
Gnomadrs121913467
Varsomers121913467
Maprs121913467
PheGenIrs121913467
Biobankrs121913467
1000 genomesrs121913467
hgdprs121913467
ensemblrs121913467
gopubmedrs121913467
geneviewrs121913467
scholarrs121913467
googlers121913467
pharmgkbrs121913467
gwascentralrs121913467
openSNPrs121913467
23andMers121913467
23andMe allrs121913467
SNP Nexus

SNPshotrs121913467
SNPdbers121913467
MSV3drs121913467
GWAS Ctlgrs121913467
Max Magnitude0
ClinVar
Risk rs121913467(A;A)
Alt rs121913467(A;A)
Reference Rs121913467(G;G)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55242423G>A
CLNSRC
CLNACC RCV000444748.1,