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rs9943582

From SNPedia

Orientationplus
Stabilizedplus
Make rs9943582(C;C)
Make rs9943582(C;T)
Make rs9943582(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position57237593
GeneAPLNR
is asnp
is mentioned by
dbSNPrs9943582
ebirs9943582
HLIrs9943582
Exacrs9943582
Varsomers9943582
Maprs9943582
PheGenIrs9943582
hapmaprs9943582
1000 genomesrs9943582
hgdprs9943582
ensemblrs9943582
gopubmedrs9943582
geneviewrs9943582
scholarrs9943582
googlers9943582
pharmgkbrs9943582
gwascentralrs9943582
openSNPrs9943582
23andMers9943582
23andMe allrs9943582
SNP Nexus

SNPshotrs9943582
SNPdbers9943582
MSV3drs9943582
GWAS Ctlgrs9943582
GMAF0.3301
Max Magnitude
? (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 25993436OA-icon.png] Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population