rs113716969
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs113716969(C;C) |
| Make rs113716969(C;T) |
| Make rs113716969(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 76812369 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs113716969 |
| dbSNP (classic) | rs113716969 |
| ClinGen | rs113716969 |
| ebi | rs113716969 |
| HLI | rs113716969 |
| Exac | rs113716969 |
| Gnomad | rs113716969 |
| Varsome | rs113716969 |
| LitVar | rs113716969 |
| Map | rs113716969 |
| PheGenI | rs113716969 |
| Biobank | rs113716969 |
| 1000 genomes | rs113716969 |
| hgdp | rs113716969 |
| ensembl | rs113716969 |
| geneview | rs113716969 |
| scholar | rs113716969 |
| rs113716969 | |
| pharmgkb | rs113716969 |
| gwascentral | rs113716969 |
| openSNP | rs113716969 |
| 23andMe | rs113716969 |
| SNPshot | rs113716969 |
| SNPdbe | rs113716969 |
| MSV3d | rs113716969 |
| GWAS Ctlg | rs113716969 |
| 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 | C |
| P-val | 2E-6 |
| Odds Ratio | .47 [0.28-0.67] unit increase |
