rs28933369

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs28933369(A;A)

Make rs28933369(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

39724744

Gene	ERBB2, MIR4728

is a	snp
is	mentioned by
dbSNP	rs28933369
dbSNP (classic)	rs28933369
ClinGen	rs28933369
ebi	rs28933369
HLI	rs28933369
Exac	rs28933369
Gnomad	rs28933369
Varsome	rs28933369
LitVar	rs28933369
Map	rs28933369
PheGenI	rs28933369
Biobank	rs28933369
1000 genomes	rs28933369
hgdp	rs28933369
ensembl	rs28933369
geneview	rs28933369
scholar	rs28933369
google	rs28933369
pharmgkb	rs28933369
gwascentral	rs28933369
openSNP	rs28933369
23andMe	rs28933369
SNPshot	rs28933369
SNPdbe	rs28933369
MSV3d	rs28933369
GWAS Ctlg	rs28933369

Max Magnitude

0

NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

OMIM	164870
Desc	GASTRIC CANCER, SOMATIC
Variant	0007
Related	also

ClinVar
Risk	rs28933369(A;A)
Alt	rs28933369(A;A)
Reference	Rs28933369(G;G)
Significance	Pathogenic
Disease	Neoplasm of stomach Adenocarcinoma of stomach Neoplasm
Variation	info
Gene	MIR4728 ERBB2
CLNDBN	Neoplasm of stomach Adenocarcinoma of stomach Neoplasm
Reversed	0
HGVS	NC_000017.10:g.37880997G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014893.5, RCV000421481.1, RCV000439112.1,