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rs397517108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs397517108(GC;TT)
Make rs397517108(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181312
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs397517108
ebirs397517108
HLIrs397517108
Exacrs397517108
Varsomers397517108
Maprs397517108
PheGenIrs397517108
hapmaprs397517108
1000 genomesrs397517108
hgdprs397517108
ensemblrs397517108
gopubmedrs397517108
geneviewrs397517108
scholarrs397517108
googlers397517108
pharmgkbrs397517108
gwascentralrs397517108
openSNPrs397517108
23andMers397517108
23andMe allrs397517108
SNP Nexus

SNPshotrs397517108
SNPdbers397517108
MSV3drs397517108
GWAS Ctlgrs397517108
Max Magnitude0
ClinVar
Risk rs397517108(TT;TT)
Alt rs397517108(TT;TT)
Reference rs397517108(GC;GC)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR EGFR-AS1
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55249005_55249006delGCinsTT
CLNSRC ClinVar
CLNACC RCV000038408.2,