rs28933369
From SNPedia
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 |
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
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, |