{{Rsnum
|rsid=2681492
|Gene=ATP2B1
|Chromosome=12
|position=89619312
|Orientation=minus
|GMAF=0.2029
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATP2B1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 78.8 | 18.6 | 2.7
| HCB | 41.9 | 47.1 | 11.0
| JPT | 31.0 | 49.6 | 19.5
| YRI | 75.9 | 21.4 | 2.8
| ASW | 77.2 | 22.8 | 0.0
| CHB | 41.9 | 47.1 | 11.0
| CHD | 38.7 | 48.1 | 13.2
| GIH | 37.6 | 45.5 | 16.8
| LWK | 62.4 | 33.0 | 4.6
| MEX | 77.6 | 20.7 | 1.7
| MKK | 0.0 | 0.0 | 0.0
| TSI | 60.4 | 37.6 | 2.0
| HapMapRevision=28
}}

[http://blog.23andme.com/2009/05/12/snpwatch-researchers-find-more-genetic-variations-associated-with-blood-pressure/ 23andMe blog] [[blood pressure]]

{{PMID Auto GWAS
|PMID=19430479
|Trait=Systolic blood pressure
|Title=Genome-wide association study of blood pressure and hypertension
|RiskAllele=T
|Pval=4E-11
|OR=0.85
|ORtxt=[0.60-1.10] mm Hg increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2681492
|overall_frequency_n=32
|overall_frequency_d=128
|overall_frequency=0.25
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=24
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23036851
|Title=Treatment factors rather than genetic variation determine metabolic syndrome in childhood cancer survivors
}}

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