{{Rsnum
|rsid=10763976
|Gene=PARD3
|Chromosome=10
|position=34564292
|Orientation=plus
|GMAF=0.3861
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.0 | 54.9 | 30.1
| HCB | 13.1 | 38.7 | 48.2
| JPT | 18.6 | 42.5 | 38.9
| YRI | 6.1 | 42.2 | 51.7
| ASW | 7.0 | 40.4 | 52.6
| CHB | 13.1 | 38.7 | 48.2
| CHD | 7.4 | 47.2 | 45.4
| GIH | 32.7 | 48.5 | 18.8
| LWK | 7.3 | 40.9 | 51.8
| MEX | 13.8 | 43.1 | 43.1
| MKK | 9.6 | 46.2 | 44.2
| TSI | 23.8 | 50.5 | 25.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=20096742
|Title=Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
}}

{{PMID Auto
|PMID=17989107
|Title=Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.
}}

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