rs3778872
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3778872(C;C) |
| Make rs3778872(C;G) |
| Make rs3778872(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 150972888 |
| Gene | KCNH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3778872 |
| dbSNP (classic) | rs3778872 |
| ClinGen | rs3778872 |
| ebi | rs3778872 |
| HLI | rs3778872 |
| Exac | rs3778872 |
| Gnomad | rs3778872 |
| Varsome | rs3778872 |
| LitVar | rs3778872 |
| Map | rs3778872 |
| PheGenI | rs3778872 |
| Biobank | rs3778872 |
| 1000 genomes | rs3778872 |
| hgdp | rs3778872 |
| ensembl | rs3778872 |
| geneview | rs3778872 |
| scholar | rs3778872 |
| rs3778872 | |
| pharmgkb | rs3778872 |
| gwascentral | rs3778872 |
| openSNP | rs3778872 |
| 23andMe | rs3778872 |
| SNPshot | rs3778872 |
| SNPdbe | rs3778872 |
| MSV3d | rs3778872 |
| GWAS Ctlg | rs3778872 |
| GMAF | 0.236 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23166209 ]
|
| Trait | QT interval |
| Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
| Risk Allele | C |
| P-val | 3E-6 |
| Odds Ratio | 1.77 [1.04-2.50] unit decrease |
