rs7784776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7784776(A;A) |
| Make rs7784776(A;G) |
| Make rs7784776(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 46580547 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7784776 |
| dbSNP (classic) | rs7784776 |
| ClinGen | rs7784776 |
| ebi | rs7784776 |
| HLI | rs7784776 |
| Exac | rs7784776 |
| Gnomad | rs7784776 |
| Varsome | rs7784776 |
| LitVar | rs7784776 |
| Map | rs7784776 |
| PheGenI | rs7784776 |
| Biobank | rs7784776 |
| 1000 genomes | rs7784776 |
| hgdp | rs7784776 |
| ensembl | rs7784776 |
| geneview | rs7784776 |
| scholar | rs7784776 |
| rs7784776 | |
| pharmgkb | rs7784776 |
| gwascentral | rs7784776 |
| openSNP | rs7784776 |
| 23andMe | rs7784776 |
| SNPshot | rs7784776 |
| SNPdbe | rs7784776 |
| MSV3d | rs7784776 |
| GWAS Ctlg | rs7784776 |
| GMAF | 0.4844 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21076409 ]
|
| Trait | |
| Title | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction |
| Risk Allele | G |
| P-val | 1E-9 |
| Odds Ratio | 0.3900 [0.25-0.53] ms increase |
[PMID 32490690] Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated with Brugada Syndrome: SADS-TW BrS Registry.
