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rs1057519847

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057519847(AG;AG)
Make rs1057519847(AG;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55191821
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519847
dbSNP (old)rs1057519847
ClinGenrs1057519847
ebirs1057519847
HLIrs1057519847
Exacrs1057519847
Gnomadrs1057519847
Varsomers1057519847
Maprs1057519847
PheGenIrs1057519847
Biobankrs1057519847
1000 genomesrs1057519847
hgdprs1057519847
ensemblrs1057519847
gopubmedrs1057519847
geneviewrs1057519847
scholarrs1057519847
googlers1057519847
pharmgkbrs1057519847
gwascentralrs1057519847
openSNPrs1057519847
23andMers1057519847
23andMe allrs1057519847
SNP Nexus

SNPshotrs1057519847
SNPdbers1057519847
MSV3drs1057519847
GWAS Ctlgrs1057519847
Max Magnitude0
ClinVar
Risk rs1057519847(AG;AG)
Alt rs1057519847(AG;AG)
Reference Rs1057519847(CT;CT)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55259514_55259515delCTinsAG
CLNSRC
CLNACC RCV000435887.1,