ARHGAP42, Rho GTPase activating protein 42, 143872

N. diseases: 25; N. variants: 14
Disease: Hypertensive disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 Biomarker group BEFREE These findings support that haploinsufficiency of ARHGAP42 leads to an age-dependent hypertension. 30903111 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 GeneticVariation group GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 GeneticVariation group BEFREE Our analysis of a well-characterized cohort of untreated borderline hypertensive patients suggested that ARHGAP42 genotype has important implications in regard to hypertension risk. 28112683 2017
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 Biomarker group BEFREE Moreover, these findings provide a potential mechanism for a hypertensive locus recently identified within arhgap42 and provide a foundation for the future development of innovative hypertension therapies. 24335996 2013
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 GeneticVariation group GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.130 GeneticVariation group GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011