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rs483352808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483352808(A;A)
Make rs483352808(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position55191720
GeneEGFR
is asnp
is mentioned by
dbSNPrs483352808
dbSNP (classic)rs483352808
ClinGenrs483352808
ebirs483352808
HLIrs483352808
Exacrs483352808
Gnomadrs483352808
Varsomers483352808
LitVarrs483352808
Maprs483352808
PheGenIrs483352808
Biobankrs483352808
1000 genomesrs483352808
hgdprs483352808
ensemblrs483352808
geneviewrs483352808
scholarrs483352808
googlers483352808
pharmgkbrs483352808
gwascentralrs483352808
openSNPrs483352808
23andMers483352808
SNPshotrs483352808
SNPdbers483352808
MSV3drs483352808
GWAS Ctlgrs483352808
Max Magnitude0
ClinVar
Risk rs483352808(A;A)
Alt rs483352808(A;A)
Reference Rs483352808(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.55259413G>A
CLNSRC ClinVar
CLNACC RCV000114406.1,