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rs397516980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516980(G;TTAT)
Make rs397516980(TTAT;TTAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724744
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516980
ebirs397516980
HLIrs397516980
Exacrs397516980
Varsomers397516980
Maprs397516980
PheGenIrs397516980
hapmaprs397516980
1000 genomesrs397516980
hgdprs397516980
ensemblrs397516980
gopubmedrs397516980
geneviewrs397516980
scholarrs397516980
googlers397516980
pharmgkbrs397516980
gwascentralrs397516980
openSNPrs397516980
23andMers397516980
23andMe allrs397516980
SNP Nexus

SNPshotrs397516980
SNPdbers397516980
MSV3drs397516980
GWAS Ctlgrs397516980
Max Magnitude0
ClinVar
Risk rs397516980(TTAT;TTAT)
Alt rs397516980(TTAT;TTAT)
Reference rs397516980(G;G)
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.37880997delGinsTTAT
CLNSRC ClinVar
CLNACC RCV000038129.2,