rs11699237
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) |
| Make rs11699237(C;T) |
| Make rs11699237(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 57108940 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11699237 |
| dbSNP (classic) | rs11699237 |
| ClinGen | rs11699237 |
| ebi | rs11699237 |
| HLI | rs11699237 |
| Exac | rs11699237 |
| Gnomad | rs11699237 |
| Varsome | rs11699237 |
| LitVar | rs11699237 |
| Map | rs11699237 |
| PheGenI | rs11699237 |
| Biobank | rs11699237 |
| 1000 genomes | rs11699237 |
| hgdp | rs11699237 |
| ensembl | rs11699237 |
| geneview | rs11699237 |
| scholar | rs11699237 |
| rs11699237 | |
| pharmgkb | rs11699237 |
| gwascentral | rs11699237 |
| openSNP | rs11699237 |
| 23andMe | rs11699237 |
| SNPshot | rs11699237 |
| SNPdbe | rs11699237 |
| MSV3d | rs11699237 |
| GWAS Ctlg | rs11699237 |
| GMAF | 0.09183 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 3E-6 |
| Odds Ratio | .12 [NR] unit increase |
