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rs121913427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913427(A;A)
Make rs121913427(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174773
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913427
dbSNP (old)rs121913427
ClinGenrs121913427
ebirs121913427
HLIrs121913427
Exacrs121913427
Gnomadrs121913427
Varsomers121913427
LitVarrs121913427
Maprs121913427
PheGenIrs121913427
Biobankrs121913427
1000 genomesrs121913427
hgdprs121913427
ensemblrs121913427
gopubmedrs121913427
geneviewrs121913427
scholarrs121913427
googlers121913427
pharmgkbrs121913427
gwascentralrs121913427
openSNPrs121913427
23andMers121913427
23andMe allrs121913427
SNPshotrs121913427
SNPdbers121913427
MSV3drs121913427
GWAS Ctlgrs121913427
Max Magnitude0
ClinVar
Risk rs121913427(A;A) rs121913427(C;C)
Alt rs121913427(A;A) rs121913427(C;C)
Reference Rs121913427(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.55242466G>A; NC_000007.13:g.55242466G>C
CLNSRC
CLNACC RCV000424472.1, RCV000154381.1,