rs2190665
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2190665(C;C) |
| Make rs2190665(C;G) |
| Make rs2190665(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78692843 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2190665 |
| dbSNP (classic) | rs2190665 |
| ClinGen | rs2190665 |
| ebi | rs2190665 |
| HLI | rs2190665 |
| Exac | rs2190665 |
| Gnomad | rs2190665 |
| Varsome | rs2190665 |
| LitVar | rs2190665 |
| Map | rs2190665 |
| PheGenI | rs2190665 |
| Biobank | rs2190665 |
| 1000 genomes | rs2190665 |
| hgdp | rs2190665 |
| ensembl | rs2190665 |
| geneview | rs2190665 |
| scholar | rs2190665 |
| rs2190665 | |
| pharmgkb | rs2190665 |
| gwascentral | rs2190665 |
| openSNP | rs2190665 |
| 23andMe | rs2190665 |
| SNPshot | rs2190665 |
| SNPdbe | rs2190665 |
| MSV3d | rs2190665 |
| GWAS Ctlg | rs2190665 |
| GMAF | 0.478 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22649501
] Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients
