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

rs121913420

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913420(A;A)
Make rs121913420(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174737
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913420
dbSNP (old)rs121913420
ClinGenrs121913420
ebirs121913420
HLIrs121913420
Exacrs121913420
Gnomadrs121913420
Varsomers121913420
Maprs121913420
PheGenIrs121913420
Biobankrs121913420
1000 genomesrs121913420
hgdprs121913420
ensemblrs121913420
gopubmedrs121913420
geneviewrs121913420
scholarrs121913420
googlers121913420
pharmgkbrs121913420
gwascentralrs121913420
openSNPrs121913420
23andMers121913420
23andMe allrs121913420
SNPshotrs121913420
SNPdbers121913420
MSV3drs121913420
GWAS Ctlgrs121913420
Max Magnitude0
ClinVar
Risk rs121913420(A;A)
Alt rs121913420(A;A)
Reference Rs121913420(G;G)
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.55242430G>A
CLNSRC
CLNACC RCV000424211.1,