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rs397516976

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516976(-;-)
Make rs397516976(-;ATACGTGATGGC)
Make rs397516976(ATACGTGATGGC;ATACGTGATGGC)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724742
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516976
ebirs397516976
HLIrs397516976
Exacrs397516976
Varsomers397516976
Maprs397516976
PheGenIrs397516976
hapmaprs397516976
1000 genomesrs397516976
hgdprs397516976
ensemblrs397516976
gopubmedrs397516976
geneviewrs397516976
scholarrs397516976
googlers397516976
pharmgkbrs397516976
gwascentralrs397516976
openSNPrs397516976
23andMers397516976
23andMe allrs397516976
SNP Nexus

SNPshotrs397516976
SNPdbers397516976
MSV3drs397516976
GWAS Ctlgrs397516976
Max Magnitude0
ClinVar
Risk rs397516976(CATACGTGATGGC,CCTCCGTGATGGC;CATACGTGATGGC,CCTCCGTGATGGC)
Alt rs397516976(CATACGTGATGGC,CCTCCGTGATGGC;CATACGTGATGGC,CCTCCGTGATGGC)
Reference rs397516976(C;C)
Significance Pathogenic
Disease Adenocarcinoma of lung Non-small cell lung cancer
Variation info
Gene MIR4728 ERBB2
CLNDBN Adenocarcinoma of lung Non-small cell lung cancer
Reversed 0
HGVS NC_000017.10:g.37880984_37880995dupATACGTGATGGC; NC_000017.10:g.37880995_37880996insCTCCGTGATGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014889.4, RCV000038123.2, RCV000156384.1,