{{Rsnum
|rsid=1458038
|Chromosome=4
|position=80243569
|Orientation=minus
|GMAF=0.2521
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 40.7 | 52.2
| HCB | 19.1 | 43.4 | 37.5
| JPT | 11.5 | 44.2 | 44.2
| YRI | 0.0 | 8.8 | 91.2
| ASW | 0.0 | 15.8 | 84.2
| CHB | 19.1 | 43.4 | 37.5
| CHD | 19.3 | 51.4 | 29.4
| GIH | 6.9 | 31.7 | 61.4
| LWK | 0.0 | 6.4 | 93.6
| MEX | 6.9 | 36.2 | 56.9
| MKK | 0.0 | 9.6 | 90.4
| TSI | 3.9 | 41.2 | 54.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=20921432
|Title=Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension. The Japanese Millennium Genome Project
}}

{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=T
|Pval=9E-25
|OR=0.4570
|ORtxt=[NR] mmHg increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=T
|Pval=3E-14
|OR=0.4030
|ORtxt=[0.30-0.51] mmHg increase
|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}}
{{on chip | NatGeo2}}