{{Rsnum
|rsid=12946454
|Gene=PLCD3
|Chromosome=17
|position=45130754
|Orientation=plus
|GMAF=0.2057
|Gene_s=ACBD4,PLCD3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 59.6 | 32.7 | 7.7
| HCB | 66.7 | 26.2 | 7.1
| JPT | 70.3 | 27.0 | 2.7
| YRI | 91.9 | 6.5 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 66.7 | 26.2 | 7.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID|19430483|OA=1
}}
[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=19430483
|Trait=Systolic blood pressure
|Title=Genome-wide association study identifies eight loci associated with blood pressure
|RiskAllele=T
|Pval=1E-8
|OR=0.57
|ORtxt=[0.37-0.77] mm Hg increase
|OA=1
}}

{{PMID Auto
|PMID=22525200
|Title=Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12946454
|overall_frequency_n=29
|overall_frequency_d=128
|overall_frequency=0.226562
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=26
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}