rs115522963
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs115522963(C;C) |
| Make rs115522963(C;T) |
| Make rs115522963(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 68806451 |
| Gene | ARHGAP25 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs115522963 |
| dbSNP (classic) | rs115522963 |
| ClinGen | rs115522963 |
| ebi | rs115522963 |
| HLI | rs115522963 |
| Exac | rs115522963 |
| Gnomad | rs115522963 |
| Varsome | rs115522963 |
| LitVar | rs115522963 |
| Map | rs115522963 |
| PheGenI | rs115522963 |
| Biobank | rs115522963 |
| 1000 genomes | rs115522963 |
| hgdp | rs115522963 |
| ensembl | rs115522963 |
| geneview | rs115522963 |
| scholar | rs115522963 |
| rs115522963 | |
| pharmgkb | rs115522963 |
| gwascentral | rs115522963 |
| openSNP | rs115522963 |
| 23andMe | rs115522963 |
| SNPshot | rs115522963 |
| SNPdbe | rs115522963 |
| MSV3d | rs115522963 |
| GWAS Ctlg | rs115522963 |
| 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 | T |
| P-val | 3E-6 |
| Odds Ratio | 1.16 [0.67-1.65] unit increase |
