rs251253
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs251253(A;A) |
| Make rs251253(A;G) |
| Make rs251253(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 173053333 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs251253 |
| dbSNP (classic) | rs251253 |
| ClinGen | rs251253 |
| ebi | rs251253 |
| HLI | rs251253 |
| Exac | rs251253 |
| Gnomad | rs251253 |
| Varsome | rs251253 |
| LitVar | rs251253 |
| Map | rs251253 |
| PheGenI | rs251253 |
| Biobank | rs251253 |
| 1000 genomes | rs251253 |
| hgdp | rs251253 |
| ensembl | rs251253 |
| geneview | rs251253 |
| scholar | rs251253 |
| rs251253 | |
| pharmgkb | rs251253 |
| gwascentral | rs251253 |
| openSNP | rs251253 |
| 23andMe | rs251253 |
| SNPshot | rs251253 |
| SNPdbe | rs251253 |
| MSV3d | rs251253 |
| GWAS Ctlg | rs251253 |
| GMAF | 0.4187 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062060 ]
|
| Trait | PR interval |
| Title | Genome-wide association study of PR interval |
| Risk Allele | C |
| P-val | 9E-13 |
| Odds Ratio | 1.49 [1.08-1.90] ms decrease |
[PMID 21347284] Genome-wide association studies of the PR interval in African Americans.
[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease
