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rs397517112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517112(-;-)
Make rs397517112(-;ACC)
Make rs397517112(ACC;ACC)
ReferenceGRCh38 38.1/141
Chromosome7
Position55181323
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs397517112
ebirs397517112
HLIrs397517112
Exacrs397517112
Varsomers397517112
Maprs397517112
PheGenIrs397517112
hapmaprs397517112
1000 genomesrs397517112
hgdprs397517112
ensemblrs397517112
gopubmedrs397517112
geneviewrs397517112
scholarrs397517112
googlers397517112
pharmgkbrs397517112
gwascentralrs397517112
openSNPrs397517112
23andMers397517112
23andMe allrs397517112
SNP Nexus

SNPshotrs397517112
SNPdbers397517112
MSV3drs397517112
GWAS Ctlgrs397517112
Max Magnitude0
ClinVar
Risk rs397517112(ACC;ACC)
Alt rs397517112(ACC;ACC)
Reference rs397517112(;)
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.55249014_55249016dupACC
CLNSRC ClinVar
CLNACC RCV000038414.2,