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rs28929495

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28929495(G;T)
Make rs28929495(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position55174014
GeneEGFR
is asnp
is mentioned by
dbSNPrs28929495
ebirs28929495
HLIrs28929495
Exacrs28929495
Varsomers28929495
Maprs28929495
PheGenIrs28929495
hapmaprs28929495
1000 genomesrs28929495
hgdprs28929495
ensemblrs28929495
gopubmedrs28929495
geneviewrs28929495
scholarrs28929495
googlers28929495
pharmgkbrs28929495
gwascentralrs28929495
openSNPrs28929495
23andMers28929495
23andMe allrs28929495
SNP Nexus

SNPshotrs28929495
SNPdbers28929495
MSV3drs28929495
GWAS Ctlgrs28929495
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM131550
DescNONSMALL CELL LUNG CANCER, RESPONSE TO TYROSINE KINASE INHIBITOR IN, SOMATIC
Variant0004
Relatedalso
OMIM131550
Desc
Variant0005
Relatedalso


ClinVar
Risk rs28929495(A,C,T;A,C,T)
Alt rs28929495(A,C,T;A,C,T)
Reference rs28929495(G;G)
Significance Drug-response
Disease Nonsmall cell lung cancer Tyrosine kinase inhibitor response Non-small cell lung cancer Squamous cell carcinoma of the head and neck
Variation info
Gene EGFR
CLNDBN Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic Tyrosine kinase inhibitor response Non-small cell lung cancer Squamous cell carcinoma of the head and neck
Reversed 0
HGVS NC_000007.13:g.55241707G>A; NC_000007.13:g.55241707G>C; NC_000007.13:g.55241707G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018087.84, RCV000154198.1, RCV000038379.2, RCV000114405.1, RCV000018086.84, RCV000038380.2,



[PMID 17956637OA-icon.png] Polymorphisms in the epidermal growth factor receptor gene and the risk of primary lung cancer: a case-control study.