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rs121434569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434569(C;T)
Make rs121434569(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181378
GeneEGFR, RPL41P5
is asnp
is mentioned by
dbSNPrs121434569
ebirs121434569
HLIrs121434569
Exacrs121434569
Varsomers121434569
Maprs121434569
PheGenIrs121434569
hapmaprs121434569
1000 genomesrs121434569
hgdprs121434569
ensemblrs121434569
gopubmedrs121434569
geneviewrs121434569
scholarrs121434569
googlers121434569
pharmgkbrs121434569
gwascentralrs121434569
openSNPrs121434569
23andMers121434569
23andMe allrs121434569
SNP Nexus

SNPshotrs121434569
SNPdbers121434569
MSV3drs121434569
GWAS Ctlgrs121434569
Max Magnitude0
OMIM131550
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121434569(T;T)
Alt rs121434569(T;T)
Reference rs121434569(C;C)
Significance Other
Disease Nonsmall cell lung cancer Tyrosine kinase inhibitor response Non-small cell lung cancer gefitinib response - Efficacy erlotinib response - Efficacy
Variation info
Gene EGFR EGFR-AS1
CLNDBN Nonsmall cell lung cancer, resistance to tyrosine kinase inhibitor in Tyrosine kinase inhibitor response Non-small cell lung cancer gefitinib response - Efficacy erlotinib response - Efficacy
Reversed 0
HGVS NC_000007.13:g.55249071C>T
CLNSRC OMIM Allelic Variant PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000018088.28, RCV000154232.1, RCV000154233.1, RCV000211140.1, RCV000211319.1,