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rs121913231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913231(C;T)
Make rs121913231(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174794
GeneEGFR
is asnp
is mentioned by
dbSNPrs121913231
dbSNP (old)rs121913231
ClinGenrs121913231
ebirs121913231
HLIrs121913231
Exacrs121913231
Gnomadrs121913231
Varsomers121913231
Maprs121913231
PheGenIrs121913231
Biobankrs121913231
1000 genomesrs121913231
hgdprs121913231
ensemblrs121913231
gopubmedrs121913231
geneviewrs121913231
scholarrs121913231
googlers121913231
pharmgkbrs121913231
gwascentralrs121913231
openSNPrs121913231
23andMers121913231
23andMe allrs121913231
SNPshotrs121913231
SNPdbers121913231
MSV3drs121913231
GWAS Ctlgrs121913231
Max Magnitude0
ClinVar
Risk rs121913231(T;T)
Alt rs121913231(T;T)
Reference Rs121913231(C;C)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer Head and Neck Neoplasms
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer Head and Neck Neoplasms
Reversed 0
HGVS NC_000007.13:g.55242487C>T
CLNSRC
CLNACC RCV000436542.1, RCV000441908.1,