{{Rsnum
|rsid=9581943
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PDX1-AS1
|position=27919860
|Gene_s=PDX1,PDX1-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 18.6 | 54.9 | 26.5
| HCB | 15.3 | 46.0 | 38.7
| JPT | 15.0 | 46.0 | 38.9
| YRI | 0.0 | 9.5 | 90.5
| ASW | 1.8 | 12.3 | 86.0
| CHB | 15.3 | 46.0 | 38.7
| CHD | 10.2 | 48.1 | 41.7
| GIH | 37.6 | 49.5 | 12.9
| LWK | 0.9 | 24.8 | 74.3
| MEX | 3.4 | 34.5 | 62.1
| MKK | 1.3 | 24.4 | 74.4
| TSI | 16.7 | 50.0 | 33.3
| HapMapRevision=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]].

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}