{{Rsnum
|rsid=16986825
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ZNRF3
|position=28904318
|Gene_s=ZNRF3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 69.0 | 28.3 | 2.7
| HCB | 36.5 | 46.7 | 16.8
| JPT | 28.3 | 52.2 | 19.5
| YRI | 97.3 | 2.0 | 0.7
| ASW | 94.7 | 5.3 | 0.0
| CHB | 36.5 | 46.7 | 16.8
| CHD | 32.4 | 50.0 | 17.6
| GIH | 47.5 | 42.6 | 9.9
| LWK | 0.0 | 0.0 | 0.0
| MEX | 62.1 | 32.8 | 5.2
| MKK | 94.2 | 5.8 | 0.0
| TSI | 64.7 | 30.4 | 4.9
| 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 [[rs16986825]](T) in [[ZNRF3]] (zinc and ring finger 3) conferring risk of statistically genome-wide significance (per-allele odds ratio (OR) = 1.18, 95% confidence interval (CI) 1.12-1.25, P = 1.2E-8) for [[Pancreatic cancer]].

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