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rs397517116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517116(-;-)
Make rs397517116(-;CACGTG)
Make rs397517116(CACGTG;CACGTG)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181331
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs397517116
ebirs397517116
HLIrs397517116
Exacrs397517116
Varsomers397517116
Maprs397517116
PheGenIrs397517116
hapmaprs397517116
1000 genomesrs397517116
hgdprs397517116
ensemblrs397517116
gopubmedrs397517116
geneviewrs397517116
scholarrs397517116
googlers397517116
pharmgkbrs397517116
gwascentralrs397517116
openSNPrs397517116
23andMers397517116
23andMe allrs397517116
SNP Nexus

SNPshotrs397517116
SNPdbers397517116
MSV3drs397517116
GWAS Ctlgrs397517116
Max Magnitude0
ClinVar
Risk rs397517116(CACGTG;CACGTG)
Alt rs397517116(CACGTG;CACGTG)
Reference rs397517116(;)
Significance Probable-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.55249019_55249024dupCACGTG
CLNSRC ClinVar
CLNACC RCV000038418.2,