rs1496770
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1496770(A;A) |
| Make rs1496770(A;G) |
| Make rs1496770(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78629694 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1496770 |
| dbSNP (classic) | rs1496770 |
| ClinGen | rs1496770 |
| ebi | rs1496770 |
| HLI | rs1496770 |
| Exac | rs1496770 |
| Gnomad | rs1496770 |
| Varsome | rs1496770 |
| LitVar | rs1496770 |
| Map | rs1496770 |
| PheGenI | rs1496770 |
| Biobank | rs1496770 |
| 1000 genomes | rs1496770 |
| hgdp | rs1496770 |
| ensembl | rs1496770 |
| geneview | rs1496770 |
| scholar | rs1496770 |
| rs1496770 | |
| pharmgkb | rs1496770 |
| gwascentral | rs1496770 |
| openSNP | rs1496770 |
| 23andMe | rs1496770 |
| SNPshot | rs1496770 |
| SNPdbe | rs1496770 |
| MSV3d | rs1496770 |
| GWAS Ctlg | rs1496770 |
| GMAF | 0.3802 |
| 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
