rs2989476
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2989476(C;C) |
| Make rs2989476(C;G) |
| Make rs2989476(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 60593587 |
| Gene | LOC105378763 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2989476 |
| dbSNP (classic) | rs2989476 |
| ClinGen | rs2989476 |
| ebi | rs2989476 |
| HLI | rs2989476 |
| Exac | rs2989476 |
| Gnomad | rs2989476 |
| Varsome | rs2989476 |
| LitVar | rs2989476 |
| Map | rs2989476 |
| PheGenI | rs2989476 |
| Biobank | rs2989476 |
| 1000 genomes | rs2989476 |
| hgdp | rs2989476 |
| ensembl | rs2989476 |
| geneview | rs2989476 |
| scholar | rs2989476 |
| rs2989476 | |
| pharmgkb | rs2989476 |
| gwascentral | rs2989476 |
| openSNP | rs2989476 |
| 23andMe | rs2989476 |
| SNPshot | rs2989476 |
| SNPdbe | rs2989476 |
| MSV3d | rs2989476 |
| GWAS Ctlg | rs2989476 |
| GMAF | 0.4844 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21738484 ]
|
| Trait | |
| Title | Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. |
| Risk Allele | C |
| P-val | 0.000003 |
| Odds Ratio | 1.1600 [NR] |
| GWAS snp | |
|---|---|
| PMID | [PMID 21254220]
|
| Trait | |
| Title | Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
[PMID 19308021] Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.
[PMID 19416921] Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.
