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rs397516981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516981(-;-)
Make rs397516981(-;GGGCTCCCC)
Make rs397516981(GGGCTCCCC;GGGCTCCCC)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724757
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516981
ebirs397516981
HLIrs397516981
Exacrs397516981
Varsomers397516981
Maprs397516981
PheGenIrs397516981
hapmaprs397516981
1000 genomesrs397516981
hgdprs397516981
ensemblrs397516981
gopubmedrs397516981
geneviewrs397516981
scholarrs397516981
googlers397516981
pharmgkbrs397516981
gwascentralrs397516981
openSNPrs397516981
23andMers397516981
23andMe allrs397516981
SNP Nexus

SNPshotrs397516981
SNPdbers397516981
MSV3drs397516981
GWAS Ctlgrs397516981
Max Magnitude0
ClinVar
Risk rs397516981(GGGCTCCCC;GGGCTCCCC)
Alt rs397516981(GGGCTCCCC;GGGCTCCCC)
Reference rs397516981(;)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene ERBB2 MIR4728
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000017.10:g.37881002_37881010dupGGGCTCCCC
CLNSRC ClinVar
CLNACC RCV000038131.2,