rs9611198
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9611198(A;A) |
| Make rs9611198(A;C) |
| Make rs9611198(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 39559868 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9611198 |
| dbSNP (classic) | rs9611198 |
| ClinGen | rs9611198 |
| ebi | rs9611198 |
| HLI | rs9611198 |
| Exac | rs9611198 |
| Gnomad | rs9611198 |
| Varsome | rs9611198 |
| LitVar | rs9611198 |
| Map | rs9611198 |
| PheGenI | rs9611198 |
| Biobank | rs9611198 |
| 1000 genomes | rs9611198 |
| hgdp | rs9611198 |
| ensembl | rs9611198 |
| geneview | rs9611198 |
| scholar | rs9611198 |
| rs9611198 | |
| pharmgkb | rs9611198 |
| gwascentral | rs9611198 |
| openSNP | rs9611198 |
| 23andMe | rs9611198 |
| SNPshot | rs9611198 |
| SNPdbe | rs9611198 |
| MSV3d | rs9611198 |
| GWAS Ctlg | rs9611198 |
| GMAF | 0.3104 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 22883433 ]
|
| Trait | Schizophrenia |
| Title | Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia. |
| Risk Allele | C |
| P-val | 8E-6 |
| Odds Ratio | 1.22 [1.11-1.34] |
