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rs28933368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28933368(A;A)
Make rs28933368(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position39725721
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs28933368
ebirs28933368
HLIrs28933368
Exacrs28933368
Varsomers28933368
Maprs28933368
PheGenIrs28933368
hapmaprs28933368
1000 genomesrs28933368
hgdprs28933368
ensemblrs28933368
gopubmedrs28933368
geneviewrs28933368
scholarrs28933368
googlers28933368
pharmgkbrs28933368
gwascentralrs28933368
openSNPrs28933368
23andMers28933368
23andMe allrs28933368
SNP Nexus

SNPshotrs28933368
SNPdbers28933368
MSV3drs28933368
GWAS Ctlgrs28933368
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM164870
DescGLIOBLASTOMA, SOMATIC
Variant0006
Relatedalso
Neighborrs28933370
Distance596


ClinVar
Risk rs28933368(A;A)
Alt rs28933368(A;A)
Reference rs28933368(G;G)
Significance Pathogenic
Disease Glioma susceptibility 1
Variation info
Gene MIR4728 ERBB2
CLNDBN Glioma susceptibility 1
Reversed 0
HGVS NC_000017.10:g.37881974G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014892.4,