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rs121913434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913434(C;T)
Make rs121913434(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position55174725
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913434
ebirs121913434
HLIrs121913434
Exacrs121913434
Varsomers121913434
Maprs121913434
PheGenIrs121913434
hapmaprs121913434
1000 genomesrs121913434
hgdprs121913434
ensemblrs121913434
gopubmedrs121913434
geneviewrs121913434
scholarrs121913434
googlers121913434
pharmgkbrs121913434
gwascentralrs121913434
openSNPrs121913434
23andMers121913434
23andMe allrs121913434
SNP Nexus

SNPshotrs121913434
SNPdbers121913434
MSV3drs121913434
GWAS Ctlgrs121913434
Max Magnitude0
ClinVar
Risk rs121913434(G,T;G,T)
Alt rs121913434(G,T;G,T)
Reference rs121913434(C;C)
Significance Drug-response
Disease Squamous cell carcinoma of the head and neck
Variation info
Gene EGFR
CLNDBN Squamous cell carcinoma of the head and neck
Reversed 0
HGVS NC_000007.13:g.55242418C>G
CLNSRC ClinVar
CLNACC RCV000114407.1,