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rs28933370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs28933370(A;G)
Make rs28933370(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position39725125
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs28933370
ebirs28933370
HLIrs28933370
Exacrs28933370
Varsomers28933370
Maprs28933370
PheGenIrs28933370
hapmaprs28933370
1000 genomesrs28933370
hgdprs28933370
ensemblrs28933370
gopubmedrs28933370
geneviewrs28933370
scholarrs28933370
googlers28933370
pharmgkbrs28933370
gwascentralrs28933370
openSNPrs28933370
23andMers28933370
23andMe allrs28933370
SNP Nexus

SNPshotrs28933370
SNPdbers28933370
MSV3drs28933370
GWAS Ctlgrs28933370
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM164870
DescOVARIAN CARCINOMA, SOMATIC
Variant0008
Relatedalso
Neighborrs28933369
Distance381
Neighborrs28933368
Distance596
? (A;A) (A;G)
ClinVar
Risk rs28933370(G;G)
Alt rs28933370(G;G)
Reference rs28933370(A;A)
Significance Pathogenic
Disease Neoplasm of ovary
Variation info
Gene MIR4728 ERBB2
CLNDBN Neoplasm of ovary
Reversed 0
HGVS NC_000017.10:g.37881378A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014894.4,