Variant: rs16948048

present in Gene: ZNF652;LOC102724596 present in Chromosome: 17 Position on Chromosome: 49363104 Alleles of this Variant: A/G

rs16948048 in ZNF652;LOC102724596 gene and Blood Pressure PMID 21378095 2011 Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.

PMID 21909110 2011 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

rs16948048 in ZNF652;LOC102724596 gene and Body Height PMID 31562340 2019 Characterizing rare and low-frequency height-associated variants in the Japanese population.

rs16948048 in ZNF652;LOC102724596 gene and Coronary Artery Disease PMID 29212778 2018 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

rs16948048 in ZNF652;LOC102724596 gene and Coronary heart disease PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs16948048 in ZNF652;LOC102724596 gene and Diastolic blood pressure PMID 19430483 2009 Genome-wide association study identifies eight loci associated with blood pressure.

PMID 27618447 2016 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.

PMID 27841878 2017 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.

rs16948048 in ZNF652;LOC102724596 gene and Diastolic blood pressure measurement PMID 19430483 2009 Genome-wide association study identifies eight loci associated with blood pressure.

rs16948048 in ZNF652;LOC102724596 gene and Malignant Neoplasms PMID 29299148 2017 Cancer risk susceptibility loci in a Swedish population.

rs16948048 in ZNF652;LOC102724596 gene and Systolic Pressure PMID 27841878 2017 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.