rs10418356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10418356(C;C) |
| Make rs10418356(C;G) |
| Make rs10418356(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 30544779 |
| Gene | ZNF536 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10418356 |
| dbSNP (classic) | rs10418356 |
| ClinGen | rs10418356 |
| ebi | rs10418356 |
| HLI | rs10418356 |
| Exac | rs10418356 |
| Gnomad | rs10418356 |
| Varsome | rs10418356 |
| LitVar | rs10418356 |
| Map | rs10418356 |
| PheGenI | rs10418356 |
| Biobank | rs10418356 |
| 1000 genomes | rs10418356 |
| hgdp | rs10418356 |
| ensembl | rs10418356 |
| geneview | rs10418356 |
| scholar | rs10418356 |
| rs10418356 | |
| pharmgkb | rs10418356 |
| gwascentral | rs10418356 |
| openSNP | rs10418356 |
| 23andMe | rs10418356 |
| SNPshot | rs10418356 |
| SNPdbe | rs10418356 |
| MSV3d | rs10418356 |
| GWAS Ctlg | rs10418356 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24159190] |
| Trait | Serum dimethylarginine levels (asymmetric) |
| Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
| Risk Allele | G |
| P-val | 7E-6 |
| Odds Ratio | .26 [0.15-0.37] unit increase |
