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rs397516978

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516978(-;-)
Make rs397516978(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724738
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516978
ebirs397516978
HLIrs397516978
Exacrs397516978
Varsomers397516978
Maprs397516978
PheGenIrs397516978
hapmaprs397516978
1000 genomesrs397516978
hgdprs397516978
ensemblrs397516978
gopubmedrs397516978
geneviewrs397516978
scholarrs397516978
googlers397516978
pharmgkbrs397516978
gwascentralrs397516978
openSNPrs397516978
23andMers397516978
23andMe allrs397516978
SNP Nexus

SNPshotrs397516978
SNPdbers397516978
MSV3drs397516978
GWAS Ctlgrs397516978
Max Magnitude0
ClinVar
Risk rs397516978(;)
Alt rs397516978(;)
Reference rs397516978(A;A)
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.37880991delA
CLNSRC ClinVar
CLNACC RCV000038125.2,