{{Rsnum
|rsid=2384550
|Chromosome=12
|position=114914926
|Orientation=plus
|GMAF=0.287
|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 | 10.6 | 52.2 | 37.2
| HCB | 1.5 | 25.5 | 73.0
| JPT | 0.9 | 17.7 | 81.4
| YRI | 10.9 | 46.3 | 42.9
| ASW | 10.5 | 33.3 | 56.1
| CHB | 1.5 | 25.5 | 73.0
| CHD | 1.8 | 28.4 | 69.7
| GIH | 16.8 | 41.6 | 41.6
| LWK | 10.0 | 48.2 | 41.8
| MEX | 12.1 | 37.9 | 50.0
| MKK | 26.9 | 44.2 | 28.8
| TSI | 21.6 | 50.0 | 28.4
| 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=Diastolic Blood Pressure
|Title=Genome-wide association study of blood pressure and hypertension
|RiskAllele=A
|Pval=4E-8
|OR=0.35
|ORtxt=[0.23-0.47] mm Hg decrease
|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=G
|Pval=0.000004
|OR=0.2270
|ORtxt=[0.13-0.32] mmHg increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2384550
|overall_frequency_n=37
|overall_frequency_d=128
|overall_frequency=0.289062
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}