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rs121913430

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913430(A;A)
Make rs121913430(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174740
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913430
dbSNP (old)rs121913430
ClinGenrs121913430
ebirs121913430
HLIrs121913430
Exacrs121913430
Gnomadrs121913430
Varsomers121913430
Maprs121913430
PheGenIrs121913430
Biobankrs121913430
1000 genomesrs121913430
hgdprs121913430
ensemblrs121913430
gopubmedrs121913430
geneviewrs121913430
scholarrs121913430
googlers121913430
pharmgkbrs121913430
gwascentralrs121913430
openSNPrs121913430
23andMers121913430
23andMe allrs121913430
SNP Nexus

SNPshotrs121913430
SNPdbers121913430
MSV3drs121913430
GWAS Ctlgrs121913430
Max Magnitude0
ClinVar
Risk rs121913430(A;A)
Alt rs121913430(A;A)
Reference Rs121913430(G;G)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer Prostatic Neoplasms
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer Prostatic Neoplasms
Reversed 0
HGVS NC_000007.13:g.55242433G>A
CLNSRC
CLNACC RCV000434054.1, RCV000442962.1,