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rs121913444

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913444(A;A)
Make rs121913444(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position55191831
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913444
ebirs121913444
HLIrs121913444
Exacrs121913444
Varsomers121913444
Maprs121913444
PheGenIrs121913444
hapmaprs121913444
1000 genomesrs121913444
hgdprs121913444
ensemblrs121913444
gopubmedrs121913444
geneviewrs121913444
scholarrs121913444
googlers121913444
pharmgkbrs121913444
gwascentralrs121913444
openSNPrs121913444
23andMers121913444
23andMe allrs121913444
SNP Nexus

SNPshotrs121913444
SNPdbers121913444
MSV3drs121913444
GWAS Ctlgrs121913444
Max Magnitude0
ClinVar
Risk rs121913444(A,G;A,G)
Alt rs121913444(A,G;A,G)
Reference rs121913444(T;T)
Significance Drug-response
Disease Tyrosine kinase inhibitor response not specified
Variation info
Gene EGFR
CLNDBN Tyrosine kinase inhibitor response not specified
Reversed 0
HGVS NC_000007.13:g.55259524T>A; NC_000007.13:g.55259524T>G
CLNSRC
CLNACC RCV000150630.1, RCV000038443.2,