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rs397516982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516982(-;-)
Make rs397516982(-;GGCTCCCCA)
Make rs397516982(GGCTCCCCA;GGCTCCCCA)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724758
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516982
ebirs397516982
HLIrs397516982
Exacrs397516982
Varsomers397516982
Maprs397516982
PheGenIrs397516982
hapmaprs397516982
1000 genomesrs397516982
hgdprs397516982
ensemblrs397516982
gopubmedrs397516982
geneviewrs397516982
scholarrs397516982
googlers397516982
pharmgkbrs397516982
gwascentralrs397516982
openSNPrs397516982
23andMers397516982
23andMe allrs397516982
SNP Nexus

SNPshotrs397516982
SNPdbers397516982
MSV3drs397516982
GWAS Ctlgrs397516982
Max Magnitude0
ClinVar
Risk rs397516982(GGCTCCCCA;GGCTCCCCA)
Alt rs397516982(GGCTCCCCA;GGCTCCCCA)
Reference rs397516982(;)
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.37881003_37881011dupGGCTCCCCA
CLNSRC ClinVar
CLNACC RCV000038132.2,