rs17691914
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17691914(A;A) |
| Make rs17691914(A;G) |
| Make rs17691914(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 34921311 |
| Gene | LOC101928135 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17691914 |
| dbSNP (classic) | rs17691914 |
| ClinGen | rs17691914 |
| ebi | rs17691914 |
| HLI | rs17691914 |
| Exac | rs17691914 |
| Gnomad | rs17691914 |
| Varsome | rs17691914 |
| LitVar | rs17691914 |
| Map | rs17691914 |
| PheGenI | rs17691914 |
| Biobank | rs17691914 |
| 1000 genomes | rs17691914 |
| hgdp | rs17691914 |
| ensembl | rs17691914 |
| geneview | rs17691914 |
| scholar | rs17691914 |
| rs17691914 | |
| pharmgkb | rs17691914 |
| gwascentral | rs17691914 |
| openSNP | rs17691914 |
| 23andMe | rs17691914 |
| SNPshot | rs17691914 |
| SNPdbe | rs17691914 |
| MSV3d | rs17691914 |
| GWAS Ctlg | rs17691914 |
| GMAF | 0.06749 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21980348
] Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery
