rs184891496
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs184891496(C;C) |
| Make rs184891496(C;T) |
| Make rs184891496(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 38750582 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs184891496 |
| dbSNP (classic) | rs184891496 |
| ClinGen | rs184891496 |
| ebi | rs184891496 |
| HLI | rs184891496 |
| Exac | rs184891496 |
| Gnomad | rs184891496 |
| Varsome | rs184891496 |
| LitVar | rs184891496 |
| Map | rs184891496 |
| PheGenI | rs184891496 |
| Biobank | rs184891496 |
| 1000 genomes | rs184891496 |
| hgdp | rs184891496 |
| ensembl | rs184891496 |
| geneview | rs184891496 |
| scholar | rs184891496 |
| rs184891496 | |
| pharmgkb | rs184891496 |
| gwascentral | rs184891496 |
| openSNP | rs184891496 |
| 23andMe | rs184891496 |
| SNPshot | rs184891496 |
| SNPdbe | rs184891496 |
| MSV3d | rs184891496 |
| GWAS Ctlg | rs184891496 |
| GMAF | 0.07622 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23319000] |
| Trait | Metabolite levels (HVA/MHPG ratio) |
| Title | Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. |
| Risk Allele | C |
| P-val | 7E-6 |
| Odds Ratio | .28 unit increase |
