rs7785088
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7785088(A;A) |
| Make rs7785088(A;G) |
| Make rs7785088(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78692296 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7785088 |
| dbSNP (classic) | rs7785088 |
| ClinGen | rs7785088 |
| ebi | rs7785088 |
| HLI | rs7785088 |
| Exac | rs7785088 |
| Gnomad | rs7785088 |
| Varsome | rs7785088 |
| LitVar | rs7785088 |
| Map | rs7785088 |
| PheGenI | rs7785088 |
| Biobank | rs7785088 |
| 1000 genomes | rs7785088 |
| hgdp | rs7785088 |
| ensembl | rs7785088 |
| geneview | rs7785088 |
| scholar | rs7785088 |
| rs7785088 | |
| pharmgkb | rs7785088 |
| gwascentral | rs7785088 |
| openSNP | rs7785088 |
| 23andMe | rs7785088 |
| SNPshot | rs7785088 |
| SNPdbe | rs7785088 |
| MSV3d | rs7785088 |
| GWAS Ctlg | rs7785088 |
| GMAF | 0.4155 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18720471
] MAGI2 genetic variation and inflammatory bowel disease.
