rs489332
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs489332(C;C) |
| Make rs489332(C;T) |
| Make rs489332(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 75413430 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs489332 |
| dbSNP (classic) | rs489332 |
| ClinGen | rs489332 |
| ebi | rs489332 |
| HLI | rs489332 |
| Exac | rs489332 |
| Gnomad | rs489332 |
| Varsome | rs489332 |
| LitVar | rs489332 |
| Map | rs489332 |
| PheGenI | rs489332 |
| Biobank | rs489332 |
| 1000 genomes | rs489332 |
| hgdp | rs489332 |
| ensembl | rs489332 |
| geneview | rs489332 |
| scholar | rs489332 |
| rs489332 | |
| pharmgkb | rs489332 |
| gwascentral | rs489332 |
| openSNP | rs489332 |
| 23andMe | rs489332 |
| SNPshot | rs489332 |
| SNPdbe | rs489332 |
| MSV3d | rs489332 |
| GWAS Ctlg | rs489332 |
| GMAF | 0.1758 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23212062 ]
|
| Trait | Schizophrenia |
| Title | Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. |
| Risk Allele | |
| P-val | 6E-6 |
| Odds Ratio | .11 [NR] unit decrease |
