rs9943582
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9943582(C;C) |
| Make rs9943582(C;T) |
| Make rs9943582(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 57237593 |
| Gene | APLNR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9943582 |
| dbSNP (classic) | rs9943582 |
| ClinGen | rs9943582 |
| ebi | rs9943582 |
| HLI | rs9943582 |
| Exac | rs9943582 |
| Gnomad | rs9943582 |
| Varsome | rs9943582 |
| LitVar | rs9943582 |
| Map | rs9943582 |
| PheGenI | rs9943582 |
| Biobank | rs9943582 |
| 1000 genomes | rs9943582 |
| hgdp | rs9943582 |
| ensembl | rs9943582 |
| geneview | rs9943582 |
| scholar | rs9943582 |
| rs9943582 | |
| pharmgkb | rs9943582 |
| gwascentral | rs9943582 |
| openSNP | rs9943582 |
| 23andMe | rs9943582 |
| SNPshot | rs9943582 |
| SNPdbe | rs9943582 |
| MSV3d | rs9943582 |
| GWAS Ctlg | rs9943582 |
| GMAF | 0.3301 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 19069168] rs2230500 (V374I) and rs9943582 were significantly associated with stroke
[PMID 19307984] Family-based analysis of apelin and AGTRL1 gene polymorphisms with hypertension in Han Chinese
[PMID 17309882] Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction.
[PMID 21358133] Genome-wide association study for ischemic stroke based on the hisayama study.
[PMID 25993436
] Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population
