rs1042714, ADRB2

N. diseases: 54
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.020 GeneticVariation BEFREE No significant association could be found between C-47T or C79G polymorphism and EH risk. 21483652 2011
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.020 GeneticVariation BEFREE No consensus has been reached on the association between the β2-adrenergic receptor polymorphisms A46G and C79G and essential hypertension risk. 20739939 2010