Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913466

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913466(C;C)
Make rs121913466(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174762
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913466
dbSNP (old)rs121913466
ClinGenrs121913466
ebirs121913466
HLIrs121913466
Exacrs121913466
Gnomadrs121913466
Varsomers121913466
Maprs121913466
PheGenIrs121913466
Biobankrs121913466
1000 genomesrs121913466
hgdprs121913466
ensemblrs121913466
gopubmedrs121913466
geneviewrs121913466
scholarrs121913466
googlers121913466
pharmgkbrs121913466
gwascentralrs121913466
openSNPrs121913466
23andMers121913466
23andMe allrs121913466
SNP Nexus

SNPshotrs121913466
SNPdbers121913466
MSV3drs121913466
GWAS Ctlgrs121913466
Max Magnitude0
ClinVar
Risk rs121913466(C;C)
Alt rs121913466(C;C)
Reference Rs121913466(T;T)
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.55242455T>C
CLNSRC
CLNACC RCV000423407.1,