rs4130590
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4130590(A;A) |
| Make rs4130590(A;G) |
| Make rs4130590(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 127345685 |
| Gene | GARNL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4130590 |
| dbSNP (classic) | rs4130590 |
| ClinGen | rs4130590 |
| ebi | rs4130590 |
| HLI | rs4130590 |
| Exac | rs4130590 |
| Gnomad | rs4130590 |
| Varsome | rs4130590 |
| LitVar | rs4130590 |
| Map | rs4130590 |
| PheGenI | rs4130590 |
| Biobank | rs4130590 |
| 1000 genomes | rs4130590 |
| hgdp | rs4130590 |
| ensembl | rs4130590 |
| geneview | rs4130590 |
| scholar | rs4130590 |
| rs4130590 | |
| pharmgkb | rs4130590 |
| gwascentral | rs4130590 |
| openSNP | rs4130590 |
| 23andMe | rs4130590 |
| SNPshot | rs4130590 |
| SNPdbe | rs4130590 |
| MSV3d | rs4130590 |
| GWAS Ctlg | rs4130590 |
| GMAF | 0.3994 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs4130590 |
| PubMedID | [PMID 18711365 ]
|
| Condition | Bipolar disorder |
| Gene | NR |
| Risk Allele | |
| pValue | 3.00E-006 |
| OR | 1.16 |
| 95% CI | |
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
