rs1349882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1349882(G;G) |
| Make rs1349882(G;T) |
| Make rs1349882(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 52722180 |
| Gene | LOC105369165 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1349882 |
| dbSNP (classic) | rs1349882 |
| ClinGen | rs1349882 |
| ebi | rs1349882 |
| HLI | rs1349882 |
| Exac | rs1349882 |
| Gnomad | rs1349882 |
| Varsome | rs1349882 |
| LitVar | rs1349882 |
| Map | rs1349882 |
| PheGenI | rs1349882 |
| Biobank | rs1349882 |
| 1000 genomes | rs1349882 |
| hgdp | rs1349882 |
| ensembl | rs1349882 |
| geneview | rs1349882 |
| scholar | rs1349882 |
| rs1349882 | |
| pharmgkb | rs1349882 |
| gwascentral | rs1349882 |
| openSNP | rs1349882 |
| 23andMe | rs1349882 |
| SNPshot | rs1349882 |
| SNPdbe | rs1349882 |
| MSV3d | rs1349882 |
| GWAS Ctlg | rs1349882 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24159190] |
| Trait | Serum dimethylarginine levels (asymmetric) |
| Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
| Risk Allele | T |
| P-val | 5E-6 |
| Odds Ratio | .09 [0.053-0.131] unit increase |
