rs184662298
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs184662298(A;A) |
| Make rs184662298(A;G) |
| Make rs184662298(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 187988099 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs184662298 |
| dbSNP (classic) | rs184662298 |
| ClinGen | rs184662298 |
| ebi | rs184662298 |
| HLI | rs184662298 |
| Exac | rs184662298 |
| Gnomad | rs184662298 |
| Varsome | rs184662298 |
| LitVar | rs184662298 |
| Map | rs184662298 |
| PheGenI | rs184662298 |
| Biobank | rs184662298 |
| 1000 genomes | rs184662298 |
| hgdp | rs184662298 |
| ensembl | rs184662298 |
| geneview | rs184662298 |
| scholar | rs184662298 |
| rs184662298 | |
| pharmgkb | rs184662298 |
| gwascentral | rs184662298 |
| openSNP | rs184662298 |
| 23andMe | rs184662298 |
| SNPshot | rs184662298 |
| SNPdbe | rs184662298 |
| MSV3d | rs184662298 |
| GWAS Ctlg | rs184662298 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24159190] |
| Trait | Serum dimethylarginine levels (asymmetric/symetric ratio) |
| Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
| Risk Allele | G |
| P-val | 3E-6 |
| Odds Ratio | 1.39 [0.8-1.97] unit increase |
