rs10491833
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10491833(C;C) |
| Make rs10491833(C;T) |
| Make rs10491833(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 24720234 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10491833 |
| dbSNP (classic) | rs10491833 |
| ClinGen | rs10491833 |
| ebi | rs10491833 |
| HLI | rs10491833 |
| Exac | rs10491833 |
| Gnomad | rs10491833 |
| Varsome | rs10491833 |
| LitVar | rs10491833 |
| Map | rs10491833 |
| PheGenI | rs10491833 |
| Biobank | rs10491833 |
| 1000 genomes | rs10491833 |
| hgdp | rs10491833 |
| ensembl | rs10491833 |
| geneview | rs10491833 |
| scholar | rs10491833 |
| rs10491833 | |
| pharmgkb | rs10491833 |
| gwascentral | rs10491833 |
| openSNP | rs10491833 |
| 23andMe | rs10491833 |
| SNPshot | rs10491833 |
| SNPdbe | rs10491833 |
| MSV3d | rs10491833 |
| GWAS Ctlg | rs10491833 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24159190] |
| Trait | Serum dimethylarginine levels (symmetric) |
| Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
| Risk Allele | C |
| P-val | 4E-6 |
| Odds Ratio | .11 [0.064-0.158] unit decrease |
