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rs121913433

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913433(A;G)
Make rs121913433(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174771
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913433
dbSNP (old)rs121913433
ClinGenrs121913433
ebirs121913433
HLIrs121913433
Exacrs121913433
Gnomadrs121913433
Varsomers121913433
Maprs121913433
PheGenIrs121913433
Biobankrs121913433
1000 genomesrs121913433
hgdprs121913433
ensemblrs121913433
gopubmedrs121913433
geneviewrs121913433
scholarrs121913433
googlers121913433
pharmgkbrs121913433
gwascentralrs121913433
openSNPrs121913433
23andMers121913433
23andMe allrs121913433
SNP Nexus

SNPshotrs121913433
SNPdbers121913433
MSV3drs121913433
GWAS Ctlgrs121913433
Max Magnitude0
ClinVar
Risk rs121913433(G;G)
Alt rs121913433(G;G)
Reference Rs121913433(A;A)
Significance Probable-Pathogenic
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.55242464A>G
CLNSRC
CLNACC RCV000433245.1,