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rs397517085

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517085(A;C)
Make rs397517085(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position55173985
GeneEGFR
is asnp
is mentioned by
dbSNPrs397517085
ebirs397517085
HLIrs397517085
Exacrs397517085
Varsomers397517085
Maprs397517085
PheGenIrs397517085
hapmaprs397517085
1000 genomesrs397517085
hgdprs397517085
ensemblrs397517085
gopubmedrs397517085
geneviewrs397517085
scholarrs397517085
googlers397517085
pharmgkbrs397517085
gwascentralrs397517085
openSNPrs397517085
23andMers397517085
23andMe allrs397517085
SNP Nexus

SNPshotrs397517085
SNPdbers397517085
MSV3drs397517085
GWAS Ctlgrs397517085
Max Magnitude0
ClinVar
Risk rs397517085(C,G,T;C,G,T)
Alt rs397517085(C,G,T;C,G,T)
Reference rs397517085(A;A)
Significance Drug-response
Disease not specified Lung cancer Tyrosine kinase inhibitor response
Variation info
Gene EGFR
CLNDBN not specified Lung cancer Tyrosine kinase inhibitor response
Reversed 0
HGVS NC_000007.13:g.55241678A>C; NC_000007.13:g.55241678A>G; NC_000007.13:g.55241678A>T
CLNSRC UniProtKB (variants)
CLNACC RCV000038374.2, RCV000206908.1, RCV000150615.1, RCV000207006.1, RCV000154197.1,