rs9581943
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9581943(A;A) |
Make rs9581943(A;G) |
Make rs9581943(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 27919860 |
Gene | PDX1, PDX1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs9581943 |
dbSNP (classic) | rs9581943 |
ClinGen | rs9581943 |
ebi | rs9581943 |
HLI | rs9581943 |
Exac | rs9581943 |
Gnomad | rs9581943 |
Varsome | rs9581943 |
LitVar | rs9581943 |
Map | rs9581943 |
PheGenI | rs9581943 |
Biobank | rs9581943 |
1000 genomes | rs9581943 |
hgdp | rs9581943 |
ensembl | rs9581943 |
geneview | rs9581943 |
scholar | rs9581943 |
rs9581943 | |
pharmgkb | rs9581943 |
gwascentral | rs9581943 |
openSNP | rs9581943 |
23andMe | rs9581943 |
SNPshot | rs9581943 |
SNPdbe | rs9581943 |
MSV3d | rs9581943 |
GWAS Ctlg | rs9581943 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
A 2014 study "Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer" of 7,683 European cases and 14,397 controls found the minor allele rs9581943(A) in PDX1 (pancreatic and duodenal homeobox 1) conferring risk of statistically genome-wide significance (per-allele odds ratio (OR) = 1.15, 95% confidence interval (CI) 1.10-1.20, P = 2.4E-9) for Pancreatic cancer.
[PMID 25086665] Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer