rs749141
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs749141(A;A) |
| Make rs749141(A;G) |
| Make rs749141(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 128571226 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs749141 |
| dbSNP (classic) | rs749141 |
| ClinGen | rs749141 |
| ebi | rs749141 |
| HLI | rs749141 |
| Exac | rs749141 |
| Gnomad | rs749141 |
| Varsome | rs749141 |
| LitVar | rs749141 |
| Map | rs749141 |
| PheGenI | rs749141 |
| Biobank | rs749141 |
| 1000 genomes | rs749141 |
| hgdp | rs749141 |
| ensembl | rs749141 |
| geneview | rs749141 |
| scholar | rs749141 |
| rs749141 | |
| pharmgkb | rs749141 |
| gwascentral | rs749141 |
| openSNP | rs749141 |
| 23andMe | rs749141 |
| SNPshot | rs749141 |
| SNPdbe | rs749141 |
| MSV3d | rs749141 |
| GWAS Ctlg | rs749141 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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-7 |
| Odds Ratio | .20 [0.12-0.27] unit increase |
