rs11047543
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs11047543(A;A) |
| Make rs11047543(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 24635405 |
| Gene | LOC105369698 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11047543 |
| dbSNP (classic) | rs11047543 |
| ClinGen | rs11047543 |
| ebi | rs11047543 |
| HLI | rs11047543 |
| Exac | rs11047543 |
| Gnomad | rs11047543 |
| Varsome | rs11047543 |
| LitVar | rs11047543 |
| Map | rs11047543 |
| PheGenI | rs11047543 |
| Biobank | rs11047543 |
| 1000 genomes | rs11047543 |
| hgdp | rs11047543 |
| ensembl | rs11047543 |
| geneview | rs11047543 |
| scholar | rs11047543 |
| rs11047543 | |
| pharmgkb | rs11047543 |
| gwascentral | rs11047543 |
| openSNP | rs11047543 |
| 23andMe | rs11047543 |
| SNPshot | rs11047543 |
| SNPdbe | rs11047543 |
| MSV3d | rs11047543 |
| GWAS Ctlg | rs11047543 |
| GMAF | 0.118 |
| 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 | A |
| P-val | 3E-13 |
| Odds Ratio | 2.09 [1.53-2.65] ms decrease |
[PMID 22336519] Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years
[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
