rs1198588
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1198588(A;A) |
| Make rs1198588(A;T) |
| Make rs1198588(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 98087276 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1198588 |
| dbSNP (classic) | rs1198588 |
| ClinGen | rs1198588 |
| ebi | rs1198588 |
| HLI | rs1198588 |
| Exac | rs1198588 |
| Gnomad | rs1198588 |
| Varsome | rs1198588 |
| LitVar | rs1198588 |
| Map | rs1198588 |
| PheGenI | rs1198588 |
| Biobank | rs1198588 |
| 1000 genomes | rs1198588 |
| hgdp | rs1198588 |
| ensembl | rs1198588 |
| geneview | rs1198588 |
| scholar | rs1198588 |
| rs1198588 | |
| pharmgkb | rs1198588 |
| gwascentral | rs1198588 |
| openSNP | rs1198588 |
| 23andMe | rs1198588 |
| SNPshot | rs1198588 |
| SNPdbe | rs1198588 |
| MSV3d | rs1198588 |
| GWAS Ctlg | rs1198588 |
| GMAF | 0.1814 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 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 | |
| P-val | 5E-7 |
| Odds Ratio | 1.1200 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 23974872]
|
| Trait | Schizophrenia |
| Title | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. |
| Risk Allele | T |
| P-val | 2E-12 |
| Odds Ratio | 1.12 [1.09-1.16] |
