rs1505368
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1505368(A;A) |
| Make rs1505368(A;G) |
| Make rs1505368(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 212432529 |
| Gene | ERBB4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1505368 |
| dbSNP (classic) | rs1505368 |
| ClinGen | rs1505368 |
| ebi | rs1505368 |
| HLI | rs1505368 |
| Exac | rs1505368 |
| Gnomad | rs1505368 |
| Varsome | rs1505368 |
| LitVar | rs1505368 |
| Map | rs1505368 |
| PheGenI | rs1505368 |
| Biobank | rs1505368 |
| 1000 genomes | rs1505368 |
| hgdp | rs1505368 |
| ensembl | rs1505368 |
| geneview | rs1505368 |
| scholar | rs1505368 |
| rs1505368 | |
| pharmgkb | rs1505368 |
| gwascentral | rs1505368 |
| openSNP | rs1505368 |
| 23andMe | rs1505368 |
| SNPshot | rs1505368 |
| SNPdbe | rs1505368 |
| MSV3d | rs1505368 |
| GWAS Ctlg | rs1505368 |
| 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 | A |
| P-val | 1E-6 |
| Odds Ratio | .10 [0.058-0.136] unit decrease |
