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rs121913443

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913443(A;A)
Make rs121913443(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55191821
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913443
dbSNP (old)rs121913443
ClinGenrs121913443
ebirs121913443
HLIrs121913443
Exacrs121913443
Gnomadrs121913443
Varsomers121913443
Maprs121913443
PheGenIrs121913443
Biobankrs121913443
1000 genomesrs121913443
hgdprs121913443
ensemblrs121913443
gopubmedrs121913443
geneviewrs121913443
scholarrs121913443
googlers121913443
pharmgkbrs121913443
gwascentralrs121913443
openSNPrs121913443
23andMers121913443
23andMe allrs121913443
SNP Nexus

SNPshotrs121913443
SNPdbers121913443
MSV3drs121913443
GWAS Ctlgrs121913443
Max Magnitude0
ClinVar
Risk rs121913443(A;A) rs121913443(T;T)
Alt rs121913443(A;A) rs121913443(T;T)
Reference Rs121913443(C;C)
Significance Probable-Pathogenic
Disease not specified Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN not specified Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55259514C>A; NC_000007.13:g.55259514C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000038439.2, RCV000431153.1, RCV000038440.2,