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rs397517094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAAGGAATTAAGAGAAGC;CAAGGAATTAAGAGAAGC) 0 common in clinvar
Make rs397517094(AAA;AAA)
Make rs397517094(AAA;CAAGGAATTAAGAGAAGC)
ReferenceGRCh38 38.1/141
Chromosome7
Position55174769
GeneEGFR
is asnp
is mentioned by
dbSNPrs397517094
dbSNP (old)rs397517094
ClinGenrs397517094
ebirs397517094
HLIrs397517094
Exacrs397517094
Varsomers397517094
Maprs397517094
PheGenIrs397517094
Biobankrs397517094
1000 genomesrs397517094
hgdprs397517094
ensemblrs397517094
gopubmedrs397517094
geneviewrs397517094
scholarrs397517094
googlers397517094
pharmgkbrs397517094
gwascentralrs397517094
openSNPrs397517094
23andMers397517094
23andMe allrs397517094
SNP Nexus

SNPshotrs397517094
SNPdbers397517094
MSV3drs397517094
GWAS Ctlgrs397517094
Max Magnitude0
ClinVar
Risk rs397517094(AAA;AAA)
Alt rs397517094(AAA;AAA)
Reference Rs397517094(CAAGGAATTAAGAGAAGC;CAAGGAATTAAGAGAAGC)
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.55242462_55242479del18insAAA
CLNSRC ClinVar
CLNACC RCV000038389.2,