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rs397516977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs397516977(-;-)
Make rs397516977(-;TACGTGATGGCT)
Make rs397516977(TACGTGATGGCT;TACGTGATGGCT)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724743
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516977
ebirs397516977
HLIrs397516977
Exacrs397516977
Varsomers397516977
Maprs397516977
PheGenIrs397516977
hapmaprs397516977
1000 genomesrs397516977
hgdprs397516977
ensemblrs397516977
gopubmedrs397516977
geneviewrs397516977
scholarrs397516977
googlers397516977
pharmgkbrs397516977
gwascentralrs397516977
openSNPrs397516977
23andMers397516977
23andMe allrs397516977
SNP Nexus

SNPshotrs397516977
SNPdbers397516977
MSV3drs397516977
GWAS Ctlgrs397516977
Max Magnitude0
ClinVar
Risk rs397516977(TTACGTGATGGCT,TTCCGTGATGGCT;TTACGTGATGGCT,TTCCGTGATGGCT)
Alt rs397516977(TTACGTGATGGCT,TTCCGTGATGGCT;TTACGTGATGGCT,TTCCGTGATGGCT)
Reference rs397516977(T;T)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene MIR4728 ERBB2
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000017.10:g.37880985_37880996dupTACGTGATGGCT; NC_000017.10:g.37880996_37880997insTCCGTGATGGCT
CLNSRC ClinVar
CLNACC RCV000038124.2, RCV000150653.1,