rs16899974
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16899974(A;A) |
| Make rs16899974(A;C) |
| Make rs16899974(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 34998772 |
| Gene | AGXT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16899974 |
| dbSNP (classic) | rs16899974 |
| ClinGen | rs16899974 |
| ebi | rs16899974 |
| HLI | rs16899974 |
| Exac | rs16899974 |
| Gnomad | rs16899974 |
| Varsome | rs16899974 |
| LitVar | rs16899974 |
| Map | rs16899974 |
| PheGenI | rs16899974 |
| Biobank | rs16899974 |
| 1000 genomes | rs16899974 |
| hgdp | rs16899974 |
| ensembl | rs16899974 |
| geneview | rs16899974 |
| scholar | rs16899974 |
| rs16899974 | |
| pharmgkb | rs16899974 |
| gwascentral | rs16899974 |
| openSNP | rs16899974 |
| 23andMe | rs16899974 |
| SNPshot | rs16899974 |
| SNPdbe | rs16899974 |
| MSV3d | rs16899974 |
| GWAS Ctlg | rs16899974 |
| GMAF | 0.2383 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 24159190] Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality
[PMID 25620171] Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population
