rs4944092
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4944092(A;A) |
| Make rs4944092(A;G) |
| Make rs4944092(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 76198575 |
| Gene | WNT11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4944092 |
| dbSNP (classic) | rs4944092 |
| ClinGen | rs4944092 |
| ebi | rs4944092 |
| HLI | rs4944092 |
| Exac | rs4944092 |
| Gnomad | rs4944092 |
| Varsome | rs4944092 |
| LitVar | rs4944092 |
| Map | rs4944092 |
| PheGenI | rs4944092 |
| Biobank | rs4944092 |
| 1000 genomes | rs4944092 |
| hgdp | rs4944092 |
| ensembl | rs4944092 |
| geneview | rs4944092 |
| scholar | rs4944092 |
| rs4944092 | |
| pharmgkb | rs4944092 |
| gwascentral | rs4944092 |
| openSNP | rs4944092 |
| 23andMe | rs4944092 |
| SNPshot | rs4944092 |
| SNPdbe | rs4944092 |
| MSV3d | rs4944092 |
| GWAS Ctlg | rs4944092 |
| GMAF | 0.3209 |
| 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 | G |
| P-val | 3E-8 |
| Odds Ratio | 1.19 [0.77-1.61] ms decrease |
[PMID 21347284] Genome-wide association studies of the PR interval in African Americans.
