rs4775892
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4775892(G;G) |
| Make rs4775892(G;T) |
| Make rs4775892(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 50600917 |
| Gene | TRPM7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4775892 |
| dbSNP (classic) | rs4775892 |
| ClinGen | rs4775892 |
| ebi | rs4775892 |
| HLI | rs4775892 |
| Exac | rs4775892 |
| Gnomad | rs4775892 |
| Varsome | rs4775892 |
| LitVar | rs4775892 |
| Map | rs4775892 |
| PheGenI | rs4775892 |
| Biobank | rs4775892 |
| 1000 genomes | rs4775892 |
| hgdp | rs4775892 |
| ensembl | rs4775892 |
| geneview | rs4775892 |
| scholar | rs4775892 |
| rs4775892 | |
| pharmgkb | rs4775892 |
| gwascentral | rs4775892 |
| openSNP | rs4775892 |
| 23andMe | rs4775892 |
| SNPshot | rs4775892 |
| SNPdbe | rs4775892 |
| MSV3d | rs4775892 |
| GWAS Ctlg | rs4775892 |
| GMAF | 0.1175 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19644062
] Gene Variation of the Transient Receptor Potential Cation Channel, Subfamily M, Member 7 (TRPM7), and Risk of Incident Ischemic Stroke. Prospective, Nested, Case-Control Study
