rs6894385
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6894385(A;A) |
| Make rs6894385(A;C) |
| Make rs6894385(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 73981078 |
| Gene | LOC105379034 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6894385 |
| dbSNP (classic) | rs6894385 |
| ClinGen | rs6894385 |
| ebi | rs6894385 |
| HLI | rs6894385 |
| Exac | rs6894385 |
| Gnomad | rs6894385 |
| Varsome | rs6894385 |
| LitVar | rs6894385 |
| Map | rs6894385 |
| PheGenI | rs6894385 |
| Biobank | rs6894385 |
| 1000 genomes | rs6894385 |
| hgdp | rs6894385 |
| ensembl | rs6894385 |
| geneview | rs6894385 |
| scholar | rs6894385 |
| rs6894385 | |
| pharmgkb | rs6894385 |
| gwascentral | rs6894385 |
| openSNP | rs6894385 |
| 23andMe | rs6894385 |
| SNPshot | rs6894385 |
| SNPdbe | rs6894385 |
| MSV3d | rs6894385 |
| GWAS Ctlg | rs6894385 |
| GMAF | 0.1731 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 1E-6 |
| Odds Ratio | 9.92 [NR] ms decrease |
