rs12666280
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12666280(C;C) |
| Make rs12666280(C;T) |
| Make rs12666280(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 154717614 |
| Gene | DPP6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12666280 |
| dbSNP (classic) | rs12666280 |
| ClinGen | rs12666280 |
| ebi | rs12666280 |
| HLI | rs12666280 |
| Exac | rs12666280 |
| Gnomad | rs12666280 |
| Varsome | rs12666280 |
| LitVar | rs12666280 |
| Map | rs12666280 |
| PheGenI | rs12666280 |
| Biobank | rs12666280 |
| 1000 genomes | rs12666280 |
| hgdp | rs12666280 |
| ensembl | rs12666280 |
| geneview | rs12666280 |
| scholar | rs12666280 |
| rs12666280 | |
| pharmgkb | rs12666280 |
| gwascentral | rs12666280 |
| openSNP | rs12666280 |
| 23andMe | rs12666280 |
| SNPshot | rs12666280 |
| SNPdbe | rs12666280 |
| MSV3d | rs12666280 |
| GWAS Ctlg | rs12666280 |
| GMAF | 0.3967 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23534349 ]
|
| Trait | QT interval |
| Title | Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans. |
| Risk Allele | C |
| P-val | 2E-6 |
| Odds Ratio | 8.93 [NR] ms increase |
