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rs397517098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAAGAGAAG;TAAGAGAAG) 0 common in clinvar
Make rs397517098(-;-)
Make rs397517098(-;TAAGAGAAG)
ReferenceGRCh38 38.1/141
Chromosome7
Position55174777
GeneEGFR
is asnp
is mentioned by
dbSNPrs397517098
ebirs397517098
HLIrs397517098
Exacrs397517098
Varsomers397517098
Maprs397517098
PheGenIrs397517098
hapmaprs397517098
1000 genomesrs397517098
hgdprs397517098
ensemblrs397517098
gopubmedrs397517098
geneviewrs397517098
scholarrs397517098
googlers397517098
pharmgkbrs397517098
gwascentralrs397517098
openSNPrs397517098
23andMers397517098
23andMe allrs397517098
SNP Nexus

SNPshotrs397517098
SNPdbers397517098
MSV3drs397517098
GWAS Ctlgrs397517098
Max Magnitude0
ClinVar
Risk rs397517098(;)
Alt rs397517098(;)
Reference rs397517098(TAAGAGAAG;TAAGAGAAG)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55242470_55242478delTAAGAGAAG
CLNSRC ClinVar
CLNACC RCV000038393.2,