rs1572299
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1572299(A;A) |
| Make rs1572299(A;G) |
| Make rs1572299(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 118584139 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1572299 |
| dbSNP (classic) | rs1572299 |
| ClinGen | rs1572299 |
| ebi | rs1572299 |
| HLI | rs1572299 |
| Exac | rs1572299 |
| Gnomad | rs1572299 |
| Varsome | rs1572299 |
| LitVar | rs1572299 |
| Map | rs1572299 |
| PheGenI | rs1572299 |
| Biobank | rs1572299 |
| 1000 genomes | rs1572299 |
| hgdp | rs1572299 |
| ensembl | rs1572299 |
| geneview | rs1572299 |
| scholar | rs1572299 |
| rs1572299 | |
| pharmgkb | rs1572299 |
| gwascentral | rs1572299 |
| openSNP | rs1572299 |
| 23andMe | rs1572299 |
| SNPshot | rs1572299 |
| SNPdbe | rs1572299 |
| MSV3d | rs1572299 |
| GWAS Ctlg | rs1572299 |
| GMAF | 0.2466 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19571808 ]
|
| Trait | Schizophrenia |
| Title | Common variants conferring risk of schizophrenia |
| Risk Allele | A |
| P-val | 0.000004 |
| Odds Ratio | 1.08 [NR] |
