rs13025591
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13025591(A;A) |
| Make rs13025591(A;C) |
| Make rs13025591(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 235886699 |
| Gene | AGAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13025591 |
| dbSNP (classic) | rs13025591 |
| ClinGen | rs13025591 |
| ebi | rs13025591 |
| HLI | rs13025591 |
| Exac | rs13025591 |
| Gnomad | rs13025591 |
| Varsome | rs13025591 |
| LitVar | rs13025591 |
| Map | rs13025591 |
| PheGenI | rs13025591 |
| Biobank | rs13025591 |
| 1000 genomes | rs13025591 |
| hgdp | rs13025591 |
| ensembl | rs13025591 |
| geneview | rs13025591 |
| scholar | rs13025591 |
| rs13025591 | |
| pharmgkb | rs13025591 |
| gwascentral | rs13025591 |
| openSNP | rs13025591 |
| 23andMe | rs13025591 |
| SNPshot | rs13025591 |
| SNPdbe | rs13025591 |
| MSV3d | rs13025591 |
| GWAS Ctlg | rs13025591 |
| GMAF | 0.4004 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21926974 ]
|
| Trait | |
| Title | Genome-wide association study identifies five new schizophrenia loci. |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | 1.0700 [1.04-1.11] |
[PMID 19571809] Common variants on chromosome 6p22.1 are associated with schizophrenia.
[PMID 20485477] New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
| 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 | 8E-8 |
| Odds Ratio | 1.1100 None |
