rs2067615
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2067615(A;A) |
| Make rs2067615(A;T) |
| Make rs2067615(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 106755644 |
| Gene | LOC100287944, RFX4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2067615 |
| dbSNP (classic) | rs2067615 |
| ClinGen | rs2067615 |
| ebi | rs2067615 |
| HLI | rs2067615 |
| Exac | rs2067615 |
| Gnomad | rs2067615 |
| Varsome | rs2067615 |
| LitVar | rs2067615 |
| Map | rs2067615 |
| PheGenI | rs2067615 |
| Biobank | rs2067615 |
| 1000 genomes | rs2067615 |
| hgdp | rs2067615 |
| ensembl | rs2067615 |
| geneview | rs2067615 |
| scholar | rs2067615 |
| rs2067615 | |
| pharmgkb | rs2067615 |
| gwascentral | rs2067615 |
| openSNP | rs2067615 |
| 23andMe | rs2067615 |
| SNPshot | rs2067615 |
| SNPdbe | rs2067615 |
| MSV3d | rs2067615 |
| GWAS Ctlg | rs2067615 |
| GMAF | 0.3981 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23583979 ]
|
| Trait | Heart rate |
| Title | Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. |
| Risk Allele | A |
| P-val | 2E-9 |
| Odds Ratio | .28 [0.19-0.36] unit increase |
