rs1484642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1484642(C;C) |
| Make rs1484642(C;G) |
| Make rs1484642(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 10129145 |
| Gene | MSRA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1484642 |
| dbSNP (classic) | rs1484642 |
| ClinGen | rs1484642 |
| ebi | rs1484642 |
| HLI | rs1484642 |
| Exac | rs1484642 |
| Gnomad | rs1484642 |
| Varsome | rs1484642 |
| LitVar | rs1484642 |
| Map | rs1484642 |
| PheGenI | rs1484642 |
| Biobank | rs1484642 |
| 1000 genomes | rs1484642 |
| hgdp | rs1484642 |
| ensembl | rs1484642 |
| geneview | rs1484642 |
| scholar | rs1484642 |
| rs1484642 | |
| pharmgkb | rs1484642 |
| gwascentral | rs1484642 |
| openSNP | rs1484642 |
| 23andMe | rs1484642 |
| SNPshot | rs1484642 |
| SNPdbe | rs1484642 |
| MSV3d | rs1484642 |
| GWAS Ctlg | rs1484642 |
| GMAF | 0.07438 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22688191 ]
|
| Trait | |
| Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
| Risk Allele | C |
| P-val | 0.000003 |
| Odds Ratio | 1.4300 None |
