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rs121913464

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913464(A;A)
Make rs121913464(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174792
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913464
dbSNP (old)rs121913464
ClinGenrs121913464
ebirs121913464
HLIrs121913464
Exacrs121913464
Gnomadrs121913464
Varsomers121913464
Maprs121913464
PheGenIrs121913464
Biobankrs121913464
1000 genomesrs121913464
hgdprs121913464
ensemblrs121913464
gopubmedrs121913464
geneviewrs121913464
scholarrs121913464
googlers121913464
pharmgkbrs121913464
gwascentralrs121913464
openSNPrs121913464
23andMers121913464
23andMe allrs121913464
SNP Nexus

SNPshotrs121913464
SNPdbers121913464
MSV3drs121913464
GWAS Ctlgrs121913464
Max Magnitude0
ClinVar
Risk rs121913464(A;A)
Alt rs121913464(A;A)
Reference Rs121913464(C;C)
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.55242485C>A
CLNSRC
CLNACC RCV000432149.1,