rs6962966
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6962966(A;A) |
| Make rs6962966(A;G) |
| Make rs6962966(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78174806 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6962966 |
| dbSNP (classic) | rs6962966 |
| ClinGen | rs6962966 |
| ebi | rs6962966 |
| HLI | rs6962966 |
| Exac | rs6962966 |
| Gnomad | rs6962966 |
| Varsome | rs6962966 |
| LitVar | rs6962966 |
| Map | rs6962966 |
| PheGenI | rs6962966 |
| Biobank | rs6962966 |
| 1000 genomes | rs6962966 |
| hgdp | rs6962966 |
| ensembl | rs6962966 |
| geneview | rs6962966 |
| scholar | rs6962966 |
| rs6962966 | |
| pharmgkb | rs6962966 |
| gwascentral | rs6962966 |
| openSNP | rs6962966 |
| 23andMe | rs6962966 |
| SNPshot | rs6962966 |
| SNPdbe | rs6962966 |
| MSV3d | rs6962966 |
| GWAS Ctlg | rs6962966 |
| GMAF | 0.4637 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20096742] Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability [PMID 17989107] Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.
[PMID 18720471
] MAGI2 genetic variation and inflammatory bowel disease.
