rs17150687
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs17150687(A;G) |
| Make rs17150687(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78413974 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17150687 |
| dbSNP (classic) | rs17150687 |
| ClinGen | rs17150687 |
| ebi | rs17150687 |
| HLI | rs17150687 |
| Exac | rs17150687 |
| Gnomad | rs17150687 |
| Varsome | rs17150687 |
| LitVar | rs17150687 |
| Map | rs17150687 |
| PheGenI | rs17150687 |
| Biobank | rs17150687 |
| 1000 genomes | rs17150687 |
| hgdp | rs17150687 |
| ensembl | rs17150687 |
| geneview | rs17150687 |
| scholar | rs17150687 |
| rs17150687 | |
| pharmgkb | rs17150687 |
| gwascentral | rs17150687 |
| openSNP | rs17150687 |
| 23andMe | rs17150687 |
| SNPshot | rs17150687 |
| SNPdbe | rs17150687 |
| MSV3d | rs17150687 |
| GWAS Ctlg | rs17150687 |
| GMAF | 0.01974 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22041458 ]
|
| Trait | |
| Title | Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D. |
| Risk Allele | C |
| P-val | 0.000003 |
| Odds Ratio | None None |
