rs181500
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs181500(A;A) |
| Make rs181500(A;C) |
| Make rs181500(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 117422360 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs181500 |
| dbSNP (classic) | rs181500 |
| ClinGen | rs181500 |
| ebi | rs181500 |
| HLI | rs181500 |
| Exac | rs181500 |
| Gnomad | rs181500 |
| Varsome | rs181500 |
| LitVar | rs181500 |
| Map | rs181500 |
| PheGenI | rs181500 |
| Biobank | rs181500 |
| 1000 genomes | rs181500 |
| hgdp | rs181500 |
| ensembl | rs181500 |
| geneview | rs181500 |
| scholar | rs181500 |
| rs181500 | |
| pharmgkb | rs181500 |
| gwascentral | rs181500 |
| openSNP | rs181500 |
| 23andMe | rs181500 |
| SNPshot | rs181500 |
| SNPdbe | rs181500 |
| MSV3d | rs181500 |
| GWAS Ctlg | rs181500 |
| GMAF | 0.3838 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22688191 ]
|
| Trait | |
| Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
| Risk Allele | T |
| P-val | 0.000005 |
| Odds Ratio | 1.2400 None |
