rs17500488
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17500488(C;C) |
| Make rs17500488(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 115669142 |
| Gene | VANGL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17500488 |
| dbSNP (classic) | rs17500488 |
| ClinGen | rs17500488 |
| ebi | rs17500488 |
| HLI | rs17500488 |
| Exac | rs17500488 |
| Gnomad | rs17500488 |
| Varsome | rs17500488 |
| LitVar | rs17500488 |
| Map | rs17500488 |
| PheGenI | rs17500488 |
| Biobank | rs17500488 |
| 1000 genomes | rs17500488 |
| hgdp | rs17500488 |
| ensembl | rs17500488 |
| geneview | rs17500488 |
| scholar | rs17500488 |
| rs17500488 | |
| pharmgkb | rs17500488 |
| gwascentral | rs17500488 |
| openSNP | rs17500488 |
| 23andMe | rs17500488 |
| SNPshot | rs17500488 |
| SNPdbe | rs17500488 |
| MSV3d | rs17500488 |
| GWAS Ctlg | rs17500488 |
| GMAF | 0.1047 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21685173
] Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease
