{{Rsnum
|rsid=2478545
|Gene=AGT
|Chromosome=1
|position=230708375
|Orientation=minus
|GMAF=0.3411
|Gene_s=AGT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 66.4 | 26.5 | 7.1
| HCB | 51.1 | 42.3 | 6.6
| JPT | 49.6 | 42.5 | 8.0
| YRI | 19.7 | 59.2 | 21.1
| ASW | 42.1 | 42.1 | 15.8
| CHB | 51.1 | 42.3 | 6.6
| CHD | 47.7 | 44.0 | 8.3
| GIH | 43.6 | 45.5 | 10.9
| LWK | 24.5 | 47.3 | 28.2
| MEX | 24.6 | 56.1 | 19.3
| MKK | 32.7 | 48.1 | 19.2
| TSI | 54.9 | 40.2 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=22739771
|Title=Genetic variation in the renin-angiotensin-aldosterone system is associated with cardiovascular risk factors and early mortality in established coronary heart disease
}}

{{PMID Auto
|PMID=19064790
|Title=Predictive genomics of cardioembolic stroke.
|OA=1
}}

{{PMID Auto
|PMID=19105203
|Title=An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
|OA=1
}}

{{PMID Auto
|PMID=20537141
|Title=Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad data.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}