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rs121913465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913465(G;T)
Make rs121913465(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181312
GeneEGFR, RPL41P5
is asnp
is mentioned by
dbSNPrs121913465
ebirs121913465
HLIrs121913465
Exacrs121913465
Varsomers121913465
Maprs121913465
PheGenIrs121913465
hapmaprs121913465
1000 genomesrs121913465
hgdprs121913465
ensemblrs121913465
gopubmedrs121913465
geneviewrs121913465
scholarrs121913465
googlers121913465
pharmgkbrs121913465
gwascentralrs121913465
openSNPrs121913465
23andMers121913465
23andMe allrs121913465
SNP Nexus

SNPshotrs121913465
SNPdbers121913465
MSV3drs121913465
GWAS Ctlgrs121913465
Max Magnitude0
ClinVar
Risk rs121913465(T;T)
Alt rs121913465(T;T)
Reference rs121913465(G;G)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR EGFR-AS1
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55249005G>T
CLNSRC COSMIC
CLNACC RCV000038407.2,