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rs397517127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517127(C;C)
Make rs397517127(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position55191749
GeneEGFR
is asnp
is mentioned by
dbSNPrs397517127
ebirs397517127
HLIrs397517127
Exacrs397517127
Varsomers397517127
Maprs397517127
PheGenIrs397517127
hapmaprs397517127
1000 genomesrs397517127
hgdprs397517127
ensemblrs397517127
gopubmedrs397517127
geneviewrs397517127
scholarrs397517127
googlers397517127
pharmgkbrs397517127
gwascentralrs397517127
openSNPrs397517127
23andMers397517127
23andMe allrs397517127
SNP Nexus

SNPshotrs397517127
SNPdbers397517127
MSV3drs397517127
GWAS Ctlgrs397517127
Max Magnitude0
ClinVar
Risk rs397517127(C,T;C,T)
Alt rs397517127(C,T;C,T)
Reference rs397517127(G;G)
Significance Pathogenic
Disease not specified Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN not specified Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55259442G>C; NC_000007.13:g.55259442G>T
CLNSRC ClinVar
CLNACC RCV000038434.2, RCV000038435.2,