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 |
---|---|---|
|
[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