{{Rsnum
|rsid=9543325
|Chromosome=13
|position=73342491
|Orientation=plus
|GMAF=0.4766
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 6.2 | 50.4 | 43.4
| HCB | 19.7 | 48.2 | 32.1
| JPT | 21.4 | 44.6 | 33.9
| YRI | 97.3 | 2.7 | 0.0
| ASW | 70.2 | 24.6 | 5.3
| CHB | 19.7 | 48.2 | 32.1
| CHD | 19.3 | 48.6 | 32.1
| GIH | 8.9 | 36.6 | 54.5
| LWK | 93.6 | 6.4 | 0.0
| MEX | 10.3 | 46.6 | 43.1
| MKK | 80.1 | 17.9 | 1.9
| TSI | 18.6 | 48.0 | 33.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20101243
|Trait=Pancreatic cancer
|Title=A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
|RiskAllele=C
|Pval=3E-11
|OR=1.26
|ORtxt=[1.18-1.35]
|OA=1
}}

The C allele of this SNP is ssociated with slightly higher risk of [[pancreatic cancer]]. {{PMID|20101243|OA=1
}}

{{omim
|id=260350
|rsnum=9543325
}}

{{PMID Auto
|PMID=22665904
|Title=A Replication Study and Genome-wide Scan of Single Nucleotide Polymorphisms Associated with Pancreatic Cancer Risk and Overall Survival
|OA=1
}}

{{PMID Auto
|PMID=20686608
|Title=Genome-wide association study of pancreatic cancer in Japanese population.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}