rs4687718
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4687718(A;A) |
| Make rs4687718(A;G) |
| Make rs4687718(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 53248287 |
| Gene | TKT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4687718 |
| dbSNP (classic) | rs4687718 |
| ClinGen | rs4687718 |
| ebi | rs4687718 |
| HLI | rs4687718 |
| Exac | rs4687718 |
| Gnomad | rs4687718 |
| Varsome | rs4687718 |
| LitVar | rs4687718 |
| Map | rs4687718 |
| PheGenI | rs4687718 |
| Biobank | rs4687718 |
| 1000 genomes | rs4687718 |
| hgdp | rs4687718 |
| ensembl | rs4687718 |
| geneview | rs4687718 |
| scholar | rs4687718 |
| rs4687718 | |
| pharmgkb | rs4687718 |
| gwascentral | rs4687718 |
| openSNP | rs4687718 |
| 23andMe | rs4687718 |
| SNPshot | rs4687718 |
| SNPdbe | rs4687718 |
| MSV3d | rs4687718 |
| GWAS Ctlg | rs4687718 |
| GMAF | 0.2048 |
| 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 | A |
| P-val | 6E-9 |
| Odds Ratio | 0.6300 [0.41-0.85] ms decrease |
[PMID 32490690] Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated with Brugada Syndrome: SADS-TW BrS Registry.
