rs16973487
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16973487(A;A) |
| Make rs16973487(A;T) |
| Make rs16973487(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 50636712 |
| Gene | TRPM7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16973487 |
| dbSNP (classic) | rs16973487 |
| ClinGen | rs16973487 |
| ebi | rs16973487 |
| HLI | rs16973487 |
| Exac | rs16973487 |
| Gnomad | rs16973487 |
| Varsome | rs16973487 |
| LitVar | rs16973487 |
| Map | rs16973487 |
| PheGenI | rs16973487 |
| Biobank | rs16973487 |
| 1000 genomes | rs16973487 |
| hgdp | rs16973487 |
| ensembl | rs16973487 |
| geneview | rs16973487 |
| scholar | rs16973487 |
| rs16973487 | |
| pharmgkb | rs16973487 |
| gwascentral | rs16973487 |
| openSNP | rs16973487 |
| 23andMe | rs16973487 |
| SNPshot | rs16973487 |
| SNPdbe | rs16973487 |
| MSV3d | rs16973487 |
| GWAS Ctlg | rs16973487 |
| GMAF | 0.1258 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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
