rs17155315
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17155315(A;A) |
| Make rs17155315(A;G) |
| Make rs17155315(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 103423957 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17155315 |
| dbSNP (classic) | rs17155315 |
| ClinGen | rs17155315 |
| ebi | rs17155315 |
| HLI | rs17155315 |
| Exac | rs17155315 |
| Gnomad | rs17155315 |
| Varsome | rs17155315 |
| LitVar | rs17155315 |
| Map | rs17155315 |
| PheGenI | rs17155315 |
| Biobank | rs17155315 |
| 1000 genomes | rs17155315 |
| hgdp | rs17155315 |
| ensembl | rs17155315 |
| geneview | rs17155315 |
| scholar | rs17155315 |
| rs17155315 | |
| pharmgkb | rs17155315 |
| gwascentral | rs17155315 |
| openSNP | rs17155315 |
| 23andMe | rs17155315 |
| SNPshot | rs17155315 |
| SNPdbe | rs17155315 |
| MSV3d | rs17155315 |
| GWAS Ctlg | rs17155315 |
| GMAF | 0.0202 |
| 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 | G |
| P-val | 7E-6 |
| Odds Ratio | 4.73 [2.69-6.77] unit increase |
