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rs483352805

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483352805(A;A)
Make rs483352805(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position55174035
GeneEGFR
is asnp
is mentioned by
dbSNPrs483352805
ebirs483352805
HLIrs483352805
Exacrs483352805
Varsomers483352805
Maprs483352805
PheGenIrs483352805
hapmaprs483352805
1000 genomesrs483352805
hgdprs483352805
ensemblrs483352805
gopubmedrs483352805
geneviewrs483352805
scholarrs483352805
googlers483352805
pharmgkbrs483352805
gwascentralrs483352805
openSNPrs483352805
23andMers483352805
23andMe allrs483352805
SNP Nexus

SNPshotrs483352805
SNPdbers483352805
MSV3drs483352805
GWAS Ctlgrs483352805
Max Magnitude0
ClinVar
Risk rs483352805(A;A)
Alt rs483352805(A;A)
Reference rs483352805(G;G)
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.55241728G>A
CLNSRC ClinVar
CLNACC RCV000114409.1,