{{Rsnum
|rsid=379742
|Chromosome=X
|position=106250703
|Orientation=minus
|GMAF=0.2461
|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 | 66.4 | 18.6 | 15.0
| HCB | 50.4 | 23.4 | 26.3
| JPT | 48.7 | 23.9 | 27.4
| YRI | 98.0 | 2.0 | 0.0
| ASW | 91.2 | 5.3 | 3.5
| CHB | 50.4 | 23.4 | 26.3
| CHD | 43.1 | 30.3 | 26.6
| GIH | 66.3 | 14.9 | 18.8
| LWK | 92.7 | 2.7 | 4.5
| MEX | 48.3 | 29.3 | 22.4
| MKK | 89.7 | 6.4 | 3.8
| TSI | 69.3 | 20.8 | 9.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23143602
  |Trait=Pancreatitis
  |Title=Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
  |RiskAllele=T
  |Pval=6E-7
  |OR=1.20
  |ORtxt=[1.10-1.30]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}