Rs2314398
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2314398 |
| PheGenI | rs2314398 |
| nextbio | rs2314398 |
| hapmap | rs2314398 |
| 1000 genomes | rs2314398 |
| hgdp | rs2314398 |
| ensembl | rs2314398 |
| gopubmed | rs2314398 |
| geneview | rs2314398 |
| scholar | rs2314398 |
| rs2314398 | |
| pharmgkb | rs2314398 |
| gwascentral | rs2314398 |
| openSNP | rs2314398 |
| 23andMe | rs2314398 |
| 23andMe all | rs2314398 |
| SNP Nexus | |
| SNPshot | rs2314398 |
| SNPdbe | rs2314398 |
| MSV3d | rs2314398 |
| Chromosome | 2 |
| Orientation | plus |
| GMAF | 0.2601 |
| Position | 97413488 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs2314398(C;C) |
| Make rs2314398(C;G) |
| Make rs2314398(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs2314398 |
| PubMedID | [PMID 18711365] |
| Condition | Bipolar disorder |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 3.00E-006 |
| OR | 1.17 |
| 95% CI | |
| GET Evidence | |
|---|---|
| rs2314398 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.179688 |
| summary | |
