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rs397509368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTAAGAGAAGCAA;TTAAGAGAAGCAA) 0 common in clinvar
Make rs397509368(C;C)
Make rs397509368(C;TTAAGAGAAGCAA)
ReferenceGRCh38 38.1/141
Chromosome7
Position55174776
GeneEGFR
is asnp
is mentioned by
dbSNPrs397509368
ebirs397509368
HLIrs397509368
Exacrs397509368
Varsomers397509368
Maprs397509368
PheGenIrs397509368
hapmaprs397509368
1000 genomesrs397509368
hgdprs397509368
ensemblrs397509368
gopubmedrs397509368
geneviewrs397509368
scholarrs397509368
googlers397509368
pharmgkbrs397509368
gwascentralrs397509368
openSNPrs397509368
23andMers397509368
23andMe allrs397509368
SNP Nexus

SNPshotrs397509368
SNPdbers397509368
MSV3drs397509368
GWAS Ctlgrs397509368
Max Magnitude0
ClinVar
Risk rs397509368(C;C)
Alt rs397509368(C;C)
Reference rs397509368(TTAAGAGAAGCAA;TTAAGAGAAGCAA)
Significance Drug-response
Disease Nonsmall cell lung cancer Tyrosine kinase inhibitor response
Variation info
Gene EGFR
CLNDBN Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic Tyrosine kinase inhibitor response
Reversed 0
HGVS NC_000007.13:g.55242469_55242481delTTAAGAGAAGCAAinsC
CLNSRC OMIM Allelic Variant
CLNACC RCV000018085.86, RCV000154240.1,