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rs397516975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516975(-;-)
Make rs397516975(-;GCATACGTGATG)
Make rs397516975(GCATACGTGATG;GCATACGTGATG)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724740
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs397516975
ebirs397516975
HLIrs397516975
Exacrs397516975
Varsomers397516975
Maprs397516975
PheGenIrs397516975
hapmaprs397516975
1000 genomesrs397516975
hgdprs397516975
ensemblrs397516975
gopubmedrs397516975
geneviewrs397516975
scholarrs397516975
googlers397516975
pharmgkbrs397516975
gwascentralrs397516975
openSNPrs397516975
23andMers397516975
23andMe allrs397516975
SNP Nexus

SNPshotrs397516975
SNPdbers397516975
MSV3drs397516975
GWAS Ctlgrs397516975
Max Magnitude0
ClinVar
Risk rs397516975(GCATACGTGATG;GCATACGTGATG)
Alt rs397516975(GCATACGTGATG;GCATACGTGATG)
Reference rs397516975(;)
Significance Pathogenic
Disease Adenocarcinoma of lung Non-small cell lung cancer
Variation info
Gene MIR4728 ERBB2
CLNDBN Adenocarcinoma of lung Non-small cell lung cancer
Reversed 0
HGVS NC_000017.10:g.37880984_37880995dupATACGTGATGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014889.4, RCV000038123.2,