rs17879755
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs17879755(C;C) |
| Make rs17879755(C;T) |
| Make rs17879755(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 3106297 |
| Gene | IL5RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17879755 |
| dbSNP (classic) | rs17879755 |
| ClinGen | rs17879755 |
| ebi | rs17879755 |
| HLI | rs17879755 |
| Exac | rs17879755 |
| Gnomad | rs17879755 |
| Varsome | rs17879755 |
| LitVar | rs17879755 |
| Map | rs17879755 |
| PheGenI | rs17879755 |
| Biobank | rs17879755 |
| 1000 genomes | rs17879755 |
| hgdp | rs17879755 |
| ensembl | rs17879755 |
| geneview | rs17879755 |
| scholar | rs17879755 |
| rs17879755 | |
| pharmgkb | rs17879755 |
| gwascentral | rs17879755 |
| openSNP | rs17879755 |
| 23andMe | rs17879755 |
| SNPshot | rs17879755 |
| SNPdbe | rs17879755 |
| MSV3d | rs17879755 |
| GWAS Ctlg | rs17879755 |
| GMAF | 0.02112 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 2E-6 |
| Odds Ratio | 5.64 [3.37-7.91] unit increase |
