{{Rsnum
|rsid=6962966
|Gene=MAGI2
|Chromosome=7
|position=78174806
|Orientation=plus
|GMAF=0.4637
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAGI2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 29.2 | 49.2 | 21.5
| HCB | 8.9 | 48.9 | 42.2
| JPT | 13.6 | 45.5 | 40.9
| YRI | 37.1 | 50.0 | 12.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 8.9 | 48.9 | 42.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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.
}}

{{PMID Auto
|PMID=18720471
|Title=MAGI2 genetic variation and inflammatory bowel disease.
|OA=1
}}