rs181519890
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs181519890(C;C) |
| Make rs181519890(C;T) |
| Make rs181519890(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 86762562 |
| Gene | PTPN13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs181519890 |
| dbSNP (classic) | rs181519890 |
| ClinGen | rs181519890 |
| ebi | rs181519890 |
| HLI | rs181519890 |
| Exac | rs181519890 |
| Gnomad | rs181519890 |
| Varsome | rs181519890 |
| LitVar | rs181519890 |
| Map | rs181519890 |
| PheGenI | rs181519890 |
| Biobank | rs181519890 |
| 1000 genomes | rs181519890 |
| hgdp | rs181519890 |
| ensembl | rs181519890 |
| geneview | rs181519890 |
| scholar | rs181519890 |
| rs181519890 | |
| pharmgkb | rs181519890 |
| gwascentral | rs181519890 |
| openSNP | rs181519890 |
| 23andMe | rs181519890 |
| SNPshot | rs181519890 |
| SNPdbe | rs181519890 |
| MSV3d | rs181519890 |
| GWAS Ctlg | rs181519890 |
| Max Magnitude | 0 |
| 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 | 6E-6 |
| Odds Ratio | 1.06 [0.60-1.52] unit increase |
