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rs397516979

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516979(-;-)
Make rs397516979(-;TCT)
Make rs397516979(TCT;TCT)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724744
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516979
ebirs397516979
HLIrs397516979
Exacrs397516979
Varsomers397516979
Maprs397516979
PheGenIrs397516979
hapmaprs397516979
1000 genomesrs397516979
hgdprs397516979
ensemblrs397516979
gopubmedrs397516979
geneviewrs397516979
scholarrs397516979
googlers397516979
pharmgkbrs397516979
gwascentralrs397516979
openSNPrs397516979
23andMers397516979
23andMe allrs397516979
SNP Nexus

SNPshotrs397516979
SNPdbers397516979
MSV3drs397516979
GWAS Ctlgrs397516979
Max Magnitude0
ClinVar
Risk rs397516979(GTCT,GTGT,GTTT;GTCT,GTGT,GTTT)
Alt rs397516979(GTCT,GTGT,GTTT;GTCT,GTGT,GTTT)
Reference rs397516979(G;G)
Significance Probable-Pathogenic
Disease not specified Non-small cell lung cancer
Variation info
Gene ERBB2 MIR4728
CLNDBN not specified Non-small cell lung cancer
Reversed 0
HGVS NC_000017.10:g.37880997_37880998insTCT; NC_000017.10:g.37880997_37880998insTGT; NC_000017.10:g.37880997_37880998insTTT
CLNSRC ClinVar
CLNACC RCV000038126.2, RCV000038127.3, RCV000038128.2,