rs2159767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2159767(C;C) |
| Make rs2159767(C;T) |
| Make rs2159767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 148299501 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2159767 |
| dbSNP (classic) | rs2159767 |
| ClinGen | rs2159767 |
| ebi | rs2159767 |
| HLI | rs2159767 |
| Exac | rs2159767 |
| Gnomad | rs2159767 |
| Varsome | rs2159767 |
| LitVar | rs2159767 |
| Map | rs2159767 |
| PheGenI | rs2159767 |
| Biobank | rs2159767 |
| 1000 genomes | rs2159767 |
| hgdp | rs2159767 |
| ensembl | rs2159767 |
| geneview | rs2159767 |
| scholar | rs2159767 |
| rs2159767 | |
| pharmgkb | rs2159767 |
| gwascentral | rs2159767 |
| openSNP | rs2159767 |
| 23andMe | rs2159767 |
| SNPshot | rs2159767 |
| SNPdbe | rs2159767 |
| MSV3d | rs2159767 |
| GWAS Ctlg | rs2159767 |
| GMAF | 0.3761 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18347602 ]
|
| Trait | Schizophrenia |
| Title | Genomewide association for schizophrenia in the CATIE study: results of stage 1 |
| Risk Allele | |
| P-val | 0.0000069999999999999999 |
| Odds Ratio | 1.33 [NR] |
