{{Rsnum
|rsid=9943582
|Gene=APLNR
|Chromosome=11
|position=57237593
|Orientation=plus
|GMAF=0.3301
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=APLNR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.9 | 39.8 | 28.3
| HCB | 54.7 | 39.4 | 5.8
| JPT | 49.6 | 38.9 | 11.5
| YRI | 54.4 | 37.4 | 8.2
| ASW | 42.1 | 45.6 | 12.3
| CHB | 54.7 | 39.4 | 5.8
| CHD | 56.0 | 40.4 | 3.7
| GIH | 54.5 | 35.6 | 9.9
| LWK | 57.3 | 35.5 | 7.3
| MEX | 43.1 | 43.1 | 13.8
| MKK | 62.2 | 30.8 | 7.1
| TSI | 40.2 | 44.1 | 15.7
| HapMapRevision=28
}}{{PMID|19069168}} [[rs2230500]] (V374I) and [[rs9943582]] were significantly associated with [[stroke]]

{{PMID Auto
|PMID=19307984
|Title=Family-based analysis of apelin and AGTRL1 gene polymorphisms with hypertension in Han Chinese
}}

{{PMID Auto
|PMID=17309882
|Title=Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction.
}}

{{PMID Auto
|PMID=21358133
|Title=Genome-wide association study for ischemic stroke based on the hisayama study.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}