rs16928297
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16928297(G;G) |
| Make rs16928297(G;T) |
| Make rs16928297(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2464890 |
| Gene | KCNQ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16928297 |
| dbSNP (classic) | rs16928297 |
| ClinGen | rs16928297 |
| ebi | rs16928297 |
| HLI | rs16928297 |
| Exac | rs16928297 |
| Gnomad | rs16928297 |
| Varsome | rs16928297 |
| LitVar | rs16928297 |
| Map | rs16928297 |
| PheGenI | rs16928297 |
| Biobank | rs16928297 |
| 1000 genomes | rs16928297 |
| hgdp | rs16928297 |
| ensembl | rs16928297 |
| geneview | rs16928297 |
| scholar | rs16928297 |
| rs16928297 | |
| pharmgkb | rs16928297 |
| gwascentral | rs16928297 |
| openSNP | rs16928297 |
| 23andMe | rs16928297 |
| SNPshot | rs16928297 |
| SNPdbe | rs16928297 |
| MSV3d | rs16928297 |
| GWAS Ctlg | rs16928297 |
| GMAF | 0.3728 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | G |
| P-val | 2E-6 |
| Odds Ratio | 1.25 [0.74-1.76] unit increase |
