rs9508025
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9508025(C;C) |
| Make rs9508025(C;G) |
| Make rs9508025(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 28409926 |
| Gene | FLT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9508025 |
| dbSNP (classic) | rs9508025 |
| ClinGen | rs9508025 |
| ebi | rs9508025 |
| HLI | rs9508025 |
| Exac | rs9508025 |
| Gnomad | rs9508025 |
| Varsome | rs9508025 |
| LitVar | rs9508025 |
| Map | rs9508025 |
| PheGenI | rs9508025 |
| Biobank | rs9508025 |
| 1000 genomes | rs9508025 |
| hgdp | rs9508025 |
| ensembl | rs9508025 |
| geneview | rs9508025 |
| scholar | rs9508025 |
| rs9508025 | |
| pharmgkb | rs9508025 |
| gwascentral | rs9508025 |
| openSNP | rs9508025 |
| 23andMe | rs9508025 |
| SNPshot | rs9508025 |
| SNPdbe | rs9508025 |
| MSV3d | rs9508025 |
| GWAS Ctlg | rs9508025 |
| GMAF | 0.3205 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23364394] A genome-wide association study of a coronary artery disease risk variant
