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rs121913229

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913229(C;C)
Make rs121913229(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174785
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913229
dbSNP (old)rs121913229
ClinGenrs121913229
ebirs121913229
HLIrs121913229
Exacrs121913229
Gnomadrs121913229
Varsomers121913229
Maprs121913229
PheGenIrs121913229
Biobankrs121913229
1000 genomesrs121913229
hgdprs121913229
ensemblrs121913229
gopubmedrs121913229
geneviewrs121913229
scholarrs121913229
googlers121913229
pharmgkbrs121913229
gwascentralrs121913229
openSNPrs121913229
23andMers121913229
23andMe allrs121913229
SNP Nexus

SNPshotrs121913229
SNPdbers121913229
MSV3drs121913229
GWAS Ctlgrs121913229
Max Magnitude0
ClinVar
Risk rs121913229(C;C)
Alt rs121913229(C;C)
Reference Rs121913229(G;G)
Significance Probable-Pathogenic
Disease not specified Non-small cell lung cancer Adenocarcinoma of lung
Variation info
Gene EGFR
CLNDBN not specified Non-small cell lung cancer Adenocarcinoma of lung
Reversed 0
HGVS NC_000007.13:g.55242478G>C
CLNSRC
CLNACC RCV000038395.2, RCV000425827.1, RCV000442888.1,