rs9984896
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9984896(A;A) |
| Make rs9984896(A;C) |
| Make rs9984896(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 36563371 |
| Gene | CLDN14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9984896 |
| dbSNP (classic) | rs9984896 |
| ClinGen | rs9984896 |
| ebi | rs9984896 |
| HLI | rs9984896 |
| Exac | rs9984896 |
| Gnomad | rs9984896 |
| Varsome | rs9984896 |
| LitVar | rs9984896 |
| Map | rs9984896 |
| PheGenI | rs9984896 |
| Biobank | rs9984896 |
| 1000 genomes | rs9984896 |
| hgdp | rs9984896 |
| ensembl | rs9984896 |
| geneview | rs9984896 |
| scholar | rs9984896 |
| rs9984896 | |
| pharmgkb | rs9984896 |
| gwascentral | rs9984896 |
| openSNP | rs9984896 |
| 23andMe | rs9984896 |
| SNPshot | rs9984896 |
| SNPdbe | rs9984896 |
| MSV3d | rs9984896 |
| GWAS Ctlg | rs9984896 |
| GMAF | 0.1175 |
| 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 | 5E-6 |
| Odds Ratio | 2.85 [1.63-4.07] unit decrease |
