rs4798896
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4798896(A;A) |
| Make rs4798896(A;G) |
| Make rs4798896(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 78152922 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4798896 |
| dbSNP (classic) | rs4798896 |
| ClinGen | rs4798896 |
| ebi | rs4798896 |
| HLI | rs4798896 |
| Exac | rs4798896 |
| Gnomad | rs4798896 |
| Varsome | rs4798896 |
| LitVar | rs4798896 |
| Map | rs4798896 |
| PheGenI | rs4798896 |
| Biobank | rs4798896 |
| 1000 genomes | rs4798896 |
| hgdp | rs4798896 |
| ensembl | rs4798896 |
| geneview | rs4798896 |
| scholar | rs4798896 |
| rs4798896 | |
| pharmgkb | rs4798896 |
| gwascentral | rs4798896 |
| openSNP | rs4798896 |
| 23andMe | rs4798896 |
| SNPshot | rs4798896 |
| SNPdbe | rs4798896 |
| MSV3d | rs4798896 |
| GWAS Ctlg | rs4798896 |
| GMAF | 0.3627 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 4E-6 |
| Odds Ratio | .09 [NR] unit increase |
