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rs121913446

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913446(C;T)
Make rs121913446(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174735
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913446
dbSNP (old)rs121913446
ClinGenrs121913446
ebirs121913446
HLIrs121913446
Exacrs121913446
Gnomadrs121913446
Varsomers121913446
Maprs121913446
PheGenIrs121913446
Biobankrs121913446
1000 genomesrs121913446
hgdprs121913446
ensemblrs121913446
gopubmedrs121913446
geneviewrs121913446
scholarrs121913446
googlers121913446
pharmgkbrs121913446
gwascentralrs121913446
openSNPrs121913446
23andMers121913446
23andMe allrs121913446
SNP Nexus

SNPshotrs121913446
SNPdbers121913446
MSV3drs121913446
GWAS Ctlgrs121913446
Max Magnitude0
ClinVar
Risk rs121913446(T;T)
Alt rs121913446(T;T)
Reference Rs121913446(C;C)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer Esophageal Squamous Cell Carcinoma
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer Esophageal Squamous Cell Carcinoma
Reversed 0
HGVS NC_000007.13:g.55242428C>T
CLNSRC
CLNACC RCV000428149.1, RCV000441469.1,