rs17206232
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17206232(A;A) |
| Make rs17206232(A;C) |
| Make rs17206232(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 65137573 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17206232 |
| dbSNP (classic) | rs17206232 |
| ClinGen | rs17206232 |
| ebi | rs17206232 |
| HLI | rs17206232 |
| Exac | rs17206232 |
| Gnomad | rs17206232 |
| Varsome | rs17206232 |
| LitVar | rs17206232 |
| Map | rs17206232 |
| PheGenI | rs17206232 |
| Biobank | rs17206232 |
| 1000 genomes | rs17206232 |
| hgdp | rs17206232 |
| ensembl | rs17206232 |
| geneview | rs17206232 |
| scholar | rs17206232 |
| rs17206232 | |
| pharmgkb | rs17206232 |
| gwascentral | rs17206232 |
| openSNP | rs17206232 |
| 23andMe | rs17206232 |
| SNPshot | rs17206232 |
| SNPdbe | rs17206232 |
| MSV3d | rs17206232 |
| GWAS Ctlg | rs17206232 |
| GMAF | 0.07897 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 1E-6 |
| Odds Ratio | .14 [NR] unit increase |
