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rs28933369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28933369(A;A)
Make rs28933369(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position39724744
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs28933369
ebirs28933369
HLIrs28933369
Exacrs28933369
Varsomers28933369
Maprs28933369
PheGenIrs28933369
hapmaprs28933369
1000 genomesrs28933369
hgdprs28933369
ensemblrs28933369
gopubmedrs28933369
geneviewrs28933369
scholarrs28933369
googlers28933369
pharmgkbrs28933369
gwascentralrs28933369
openSNPrs28933369
23andMers28933369
23andMe allrs28933369
SNP Nexus

SNPshotrs28933369
SNPdbers28933369
MSV3drs28933369
GWAS Ctlgrs28933369
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM164870
DescGASTRIC CANCER, SOMATIC
Variant0007
Relatedalso
Neighborrs28933370
Distance381


ClinVar
Risk rs28933369(A;A)
Alt rs28933369(A;A)
Reference rs28933369(G;G)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene ERBB2 MIR4728
CLNDBN Neoplasm of stomach
Reversed 0
HGVS NC_000017.10:g.37880997G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014893.4,