rs11008099
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11008099(A;A) |
| Make rs11008099(A;G) |
| Make rs11008099(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 30545703 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11008099 |
| dbSNP (classic) | rs11008099 |
| ClinGen | rs11008099 |
| ebi | rs11008099 |
| HLI | rs11008099 |
| Exac | rs11008099 |
| Gnomad | rs11008099 |
| Varsome | rs11008099 |
| LitVar | rs11008099 |
| Map | rs11008099 |
| PheGenI | rs11008099 |
| Biobank | rs11008099 |
| 1000 genomes | rs11008099 |
| hgdp | rs11008099 |
| ensembl | rs11008099 |
| geneview | rs11008099 |
| scholar | rs11008099 |
| rs11008099 | |
| pharmgkb | rs11008099 |
| gwascentral | rs11008099 |
| openSNP | rs11008099 |
| 23andMe | rs11008099 |
| SNPshot | rs11008099 |
| SNPdbe | rs11008099 |
| MSV3d | rs11008099 |
| GWAS Ctlg | rs11008099 |
| GMAF | 0.1028 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | A |
| P-val | 9E-6 |
| Odds Ratio | 2.74 [1.54-3.94] unit increase |
