rs17645523
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17645523(C;C) |
| Make rs17645523(C;T) |
| Make rs17645523(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 50590448 |
| Gene | TRPM7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17645523 |
| dbSNP (classic) | rs17645523 |
| ClinGen | rs17645523 |
| ebi | rs17645523 |
| HLI | rs17645523 |
| Exac | rs17645523 |
| Gnomad | rs17645523 |
| Varsome | rs17645523 |
| LitVar | rs17645523 |
| Map | rs17645523 |
| PheGenI | rs17645523 |
| Biobank | rs17645523 |
| 1000 genomes | rs17645523 |
| hgdp | rs17645523 |
| ensembl | rs17645523 |
| geneview | rs17645523 |
| scholar | rs17645523 |
| rs17645523 | |
| pharmgkb | rs17645523 |
| gwascentral | rs17645523 |
| openSNP | rs17645523 |
| 23andMe | rs17645523 |
| SNPshot | rs17645523 |
| SNPdbe | rs17645523 |
| MSV3d | rs17645523 |
| GWAS Ctlg | rs17645523 |
| GMAF | 0.4077 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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
