rs7660702
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7660702(C;C) |
| Make rs7660702(C;T) |
| Make rs7660702(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 85730311 |
| Gene | ARHGAP24 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7660702 |
| dbSNP (classic) | rs7660702 |
| ClinGen | rs7660702 |
| ebi | rs7660702 |
| HLI | rs7660702 |
| Exac | rs7660702 |
| Gnomad | rs7660702 |
| Varsome | rs7660702 |
| LitVar | rs7660702 |
| Map | rs7660702 |
| PheGenI | rs7660702 |
| Biobank | rs7660702 |
| 1000 genomes | rs7660702 |
| hgdp | rs7660702 |
| ensembl | rs7660702 |
| geneview | rs7660702 |
| scholar | rs7660702 |
| rs7660702 | |
| pharmgkb | rs7660702 |
| gwascentral | rs7660702 |
| openSNP | rs7660702 |
| 23andMe | rs7660702 |
| SNPshot | rs7660702 |
| SNPdbe | rs7660702 |
| MSV3d | rs7660702 |
| GWAS Ctlg | rs7660702 |
| GMAF | 0.4284 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062063] |
| Trait | Electrocardiographic traits |
| Title | Several common variants modulate heart rate, PR interval and QRS duration |
| Risk Allele | T |
| P-val | 3E-17 |
| Odds Ratio | 8.46 [6.50-10.42] % SD increase |
[PMID 21347284
] Genome-wide association studies of the PR interval in African Americans.
