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rs121913418

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913418(A;A)
Make rs121913418(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174818
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913418
dbSNP (old)rs121913418
ClinGenrs121913418
ebirs121913418
HLIrs121913418
Exacrs121913418
Gnomadrs121913418
Varsomers121913418
Maprs121913418
PheGenIrs121913418
Biobankrs121913418
1000 genomesrs121913418
hgdprs121913418
ensemblrs121913418
gopubmedrs121913418
geneviewrs121913418
scholarrs121913418
googlers121913418
pharmgkbrs121913418
gwascentralrs121913418
openSNPrs121913418
23andMers121913418
23andMe allrs121913418
SNP Nexus

SNPshotrs121913418
SNPdbers121913418
MSV3drs121913418
GWAS Ctlgrs121913418
Max Magnitude0
ClinVar
Risk rs121913418(A;A) rs121913418(T;T)
Alt rs121913418(A;A) rs121913418(T;T)
Reference Rs121913418(G;G)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer not specified
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer not specified
Reversed 0
HGVS NC_000007.13:g.55242511G>A; NC_000007.13:g.55242511G>T
CLNSRC
CLNACC RCV000425618.1, RCV000038400.2, RCV000435465.1,