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rs397517111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517111(-;-)
Make rs397517111(-;GGGTTG)
Make rs397517111(GGGTTG;GGGTTG)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181319
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs397517111
ebirs397517111
HLIrs397517111
Exacrs397517111
Varsomers397517111
Maprs397517111
PheGenIrs397517111
hapmaprs397517111
1000 genomesrs397517111
hgdprs397517111
ensemblrs397517111
gopubmedrs397517111
geneviewrs397517111
scholarrs397517111
googlers397517111
pharmgkbrs397517111
gwascentralrs397517111
openSNPrs397517111
23andMers397517111
23andMe allrs397517111
SNP Nexus

SNPshotrs397517111
SNPdbers397517111
MSV3drs397517111
GWAS Ctlgrs397517111
Max Magnitude0
ClinVar
Risk rs397517111(GGGTTG;GGGTTG)
Alt rs397517111(GGGTTG;GGGTTG)
Reference rs397517111(;)
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.55249012_55249013insGGGTTG
CLNSRC ClinVar
CLNACC RCV000038413.2,