rs349475
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs349475(A;A) |
| Make rs349475(A;G) |
| Make rs349475(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 19440059 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs349475 |
| dbSNP (classic) | rs349475 |
| ClinGen | rs349475 |
| ebi | rs349475 |
| HLI | rs349475 |
| Exac | rs349475 |
| Gnomad | rs349475 |
| Varsome | rs349475 |
| LitVar | rs349475 |
| Map | rs349475 |
| PheGenI | rs349475 |
| Biobank | rs349475 |
| 1000 genomes | rs349475 |
| hgdp | rs349475 |
| ensembl | rs349475 |
| geneview | rs349475 |
| scholar | rs349475 |
| rs349475 | |
| pharmgkb | rs349475 |
| gwascentral | rs349475 |
| openSNP | rs349475 |
| 23andMe | rs349475 |
| SNPshot | rs349475 |
| SNPdbe | rs349475 |
| MSV3d | rs349475 |
| GWAS Ctlg | rs349475 |
| GMAF | 0.3724 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20800221 ]
|
| Trait | |
| Title | Genome-Wide Association Scan of Trait Depression |
| Risk Allele | T |
| P-val | 0.000002 |
| Odds Ratio | 0.18 [NR] unit increase |
