rs28933379
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs28933379(A;A) |
Make rs28933379(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112838953 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs28933379 |
dbSNP (classic) | rs28933379 |
ClinGen | rs28933379 |
ebi | rs28933379 |
HLI | rs28933379 |
Exac | rs28933379 |
Gnomad | rs28933379 |
Varsome | rs28933379 |
LitVar | rs28933379 |
Map | rs28933379 |
PheGenI | rs28933379 |
Biobank | rs28933379 |
1000 genomes | rs28933379 |
hgdp | rs28933379 |
ensembl | rs28933379 |
geneview | rs28933379 |
scholar | rs28933379 |
rs28933379 | |
pharmgkb | rs28933379 |
gwascentral | rs28933379 |
openSNP | rs28933379 |
23andMe | rs28933379 |
SNPshot | rs28933379 |
SNPdbe | rs28933379 |
MSV3d | rs28933379 |
GWAS Ctlg | rs28933379 |
Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
ClinVar | |
---|---|
Risk | rs28933379(A;A) |
Alt | rs28933379(A;A) |
Reference | Rs28933379(G;G) |
Significance | Pathogenic |
Disease | Neoplasm of stomach |
Variation | info |
Gene | APC |
CLNDBN | Neoplasm of stomach |
Reversed | 0 |
HGVS | NC_000005.9:g.112174650G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000839.4, |