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rs397517086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAC;AAC) 0 common in clinvar
Make rs397517086(-;-)
Make rs397517086(-;AAC)
ReferenceGRCh38 38.1/141
Chromosome7
Position55173986
GeneEGFR
is asnp
is mentioned by
dbSNPrs397517086
ebirs397517086
HLIrs397517086
Exacrs397517086
Varsomers397517086
Maprs397517086
PheGenIrs397517086
hapmaprs397517086
1000 genomesrs397517086
hgdprs397517086
ensemblrs397517086
gopubmedrs397517086
geneviewrs397517086
scholarrs397517086
googlers397517086
pharmgkbrs397517086
gwascentralrs397517086
openSNPrs397517086
23andMers397517086
23andMe allrs397517086
SNP Nexus

SNPshotrs397517086
SNPdbers397517086
MSV3drs397517086
GWAS Ctlgrs397517086
Max Magnitude0
ClinVar
Risk rs397517086(;)
Alt rs397517086(;)
Reference rs397517086(AAC;AAC)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55241679_55241681delAAC
CLNSRC COSMIC
CLNACC RCV000038375.2,