rs1000589
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1000589(G;G) |
Make rs1000589(G;T) |
Make rs1000589(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 63567780 |
is a | snp |
is | mentioned by |
dbSNP | rs1000589 |
dbSNP (classic) | rs1000589 |
ClinGen | rs1000589 |
ebi | rs1000589 |
HLI | rs1000589 |
Exac | rs1000589 |
Gnomad | rs1000589 |
Varsome | rs1000589 |
LitVar | rs1000589 |
Map | rs1000589 |
PheGenI | rs1000589 |
Biobank | rs1000589 |
1000 genomes | rs1000589 |
hgdp | rs1000589 |
ensembl | rs1000589 |
geneview | rs1000589 |
scholar | rs1000589 |
rs1000589 | |
pharmgkb | rs1000589 |
gwascentral | rs1000589 |
openSNP | rs1000589 |
23andMe | rs1000589 |
SNPshot | rs1000589 |
SNPdbe | rs1000589 |
MSV3d | rs1000589 |
GWAS Ctlg | rs1000589 |
GMAF | 0.4729 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23180869] |
Trait | Pancreatic cancer |
Title | Genome-wide association study of survival in patients with pancreatic adenocarcinoma. |
Risk Allele | T |
P-val | 3E-6 |
Odds Ratio | 1.27 [1.15-1.39] |