rs9866825
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9866825(A;A) |
| Make rs9866825(A;C) |
| Make rs9866825(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 8209103 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9866825 |
| dbSNP (classic) | rs9866825 |
| ClinGen | rs9866825 |
| ebi | rs9866825 |
| HLI | rs9866825 |
| Exac | rs9866825 |
| Gnomad | rs9866825 |
| Varsome | rs9866825 |
| LitVar | rs9866825 |
| Map | rs9866825 |
| PheGenI | rs9866825 |
| Biobank | rs9866825 |
| 1000 genomes | rs9866825 |
| hgdp | rs9866825 |
| ensembl | rs9866825 |
| geneview | rs9866825 |
| scholar | rs9866825 |
| rs9866825 | |
| pharmgkb | rs9866825 |
| gwascentral | rs9866825 |
| openSNP | rs9866825 |
| 23andMe | rs9866825 |
| SNPshot | rs9866825 |
| SNPdbe | rs9866825 |
| MSV3d | rs9866825 |
| GWAS Ctlg | rs9866825 |
| GMAF | 0.3999 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | A |
| P-val | 8E-6 |
| Odds Ratio | 1.18 [0.67-1.69] unit increase |
