rs3010396
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3010396(A;A) |
| Make rs3010396(A;G) |
| Make rs3010396(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 115731167 |
| Gene | CASQ2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3010396 |
| dbSNP (classic) | rs3010396 |
| ClinGen | rs3010396 |
| ebi | rs3010396 |
| HLI | rs3010396 |
| Exac | rs3010396 |
| Gnomad | rs3010396 |
| Varsome | rs3010396 |
| LitVar | rs3010396 |
| Map | rs3010396 |
| PheGenI | rs3010396 |
| Biobank | rs3010396 |
| 1000 genomes | rs3010396 |
| hgdp | rs3010396 |
| ensembl | rs3010396 |
| geneview | rs3010396 |
| scholar | rs3010396 |
| rs3010396 | |
| pharmgkb | rs3010396 |
| gwascentral | rs3010396 |
| openSNP | rs3010396 |
| 23andMe | rs3010396 |
| SNPshot | rs3010396 |
| SNPdbe | rs3010396 |
| MSV3d | rs3010396 |
| GWAS Ctlg | rs3010396 |
| GMAF | 0.3512 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21685173
] Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease
