{{Rsnum
|rsid=16948048
|Gene=ZNF652
|Chromosome=17
|position=49363104
|Orientation=plus
|GMAF=0.3113
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LOC102724596,RP11-1079K10.3,ZNF652
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.6 | 49.6 | 16.8
| HCB | 67.2 | 29.2 | 3.6
| JPT | 78.8 | 20.4 | 0.9
| YRI | 34.2 | 52.1 | 13.7
| ASW | 38.6 | 49.1 | 12.3
| CHB | 67.2 | 29.2 | 3.6
| CHD | 60.6 | 33.9 | 5.5
| GIH | 70.3 | 26.7 | 3.0
| LWK | 40.9 | 44.5 | 14.5
| MEX | 50.0 | 44.8 | 5.2
| MKK | 48.7 | 37.2 | 14.1
| TSI | 50.0 | 38.2 | 11.8
| 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=19430483
|Trait=Diastolic Blood Pressure
|Title=Genome-wide association study identifies eight loci associated with blood pressure
|RiskAllele=G
|Pval=5E-9
|OR=0.31
|ORtxt=[0.21-0.41] mm Hg increase
|OA=1
}}

{{PMID|20542020}} Confirmation of top polymorphisms in hypertension genome wide association study among Han Chinese.

{{PMID|22525200}} 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=rs16948048
|overall_frequency_n=41
|overall_frequency_d=128
|overall_frequency=0.320312
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=36
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}