rs3782889
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3782889(C;C) |
| Make rs3782889(C;T) |
| Make rs3782889(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 110912851 |
| Gene | MYL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3782889 |
| dbSNP (classic) | rs3782889 |
| ClinGen | rs3782889 |
| ebi | rs3782889 |
| HLI | rs3782889 |
| Exac | rs3782889 |
| Gnomad | rs3782889 |
| Varsome | rs3782889 |
| LitVar | rs3782889 |
| Map | rs3782889 |
| PheGenI | rs3782889 |
| Biobank | rs3782889 |
| 1000 genomes | rs3782889 |
| hgdp | rs3782889 |
| ensembl | rs3782889 |
| geneview | rs3782889 |
| scholar | rs3782889 |
| rs3782889 | |
| pharmgkb | rs3782889 |
| gwascentral | rs3782889 |
| openSNP | rs3782889 |
| 23andMe | rs3782889 |
| SNPshot | rs3782889 |
| SNPdbe | rs3782889 |
| MSV3d | rs3782889 |
| GWAS Ctlg | rs3782889 |
| GMAF | 0.09826 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23364394] A genome-wide association study of a coronary artery disease risk variant
