rs2020744
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2020744(G;G) |
| Make rs2020744(G;T) |
| Make rs2020744(T;T) |
| Reference | GRCm38 38.1/137 |
| Chromosome | 14 |
| Position | 11204258 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2020744 |
| dbSNP (classic) | rs2020744 |
| ClinGen | rs2020744 |
| ebi | rs2020744 |
| HLI | rs2020744 |
| Exac | rs2020744 |
| Gnomad | rs2020744 |
| Varsome | rs2020744 |
| LitVar | rs2020744 |
| Map | rs2020744 |
| PheGenI | rs2020744 |
| Biobank | rs2020744 |
| 1000 genomes | rs2020744 |
| hgdp | rs2020744 |
| ensembl | rs2020744 |
| geneview | rs2020744 |
| scholar | rs2020744 |
| rs2020744 | |
| pharmgkb | rs2020744 |
| gwascentral | rs2020744 |
| openSNP | rs2020744 |
| 23andMe | rs2020744 |
| SNPshot | rs2020744 |
| SNPdbe | rs2020744 |
| MSV3d | rs2020744 |
| GWAS Ctlg | rs2020744 |
| Max Magnitude | 0 |
[PMID 21963893
] Polymorphisms of genes in nitric oxide-forming pathway associated with ischemic stroke in Chinese Han population
