rs9640699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9640699(A;A) |
| Make rs9640699(A;C) |
| Make rs9640699(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78366115 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9640699 |
| dbSNP (classic) | rs9640699 |
| ClinGen | rs9640699 |
| ebi | rs9640699 |
| HLI | rs9640699 |
| Exac | rs9640699 |
| Gnomad | rs9640699 |
| Varsome | rs9640699 |
| LitVar | rs9640699 |
| Map | rs9640699 |
| PheGenI | rs9640699 |
| Biobank | rs9640699 |
| 1000 genomes | rs9640699 |
| hgdp | rs9640699 |
| ensembl | rs9640699 |
| geneview | rs9640699 |
| scholar | rs9640699 |
| rs9640699 | |
| pharmgkb | rs9640699 |
| gwascentral | rs9640699 |
| openSNP | rs9640699 |
| 23andMe | rs9640699 |
| SNPshot | rs9640699 |
| SNPdbe | rs9640699 |
| MSV3d | rs9640699 |
| GWAS Ctlg | rs9640699 |
| GMAF | 0.4674 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20096742] Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
