rs1042713, ADRB2

N. diseases: 63
Disease: Heart failure ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Heart failure
CUI: C0018801
Disease: Heart failure
0.040 GeneticVariation BEFREE ADRB2 polymorphism Arg16Gly modifies the natural outcome of heart failure and dictates therapeutic response to β-blockers in patients with heart failure. 30374408 2018
Heart failure
CUI: C0018801
Disease: Heart failure
0.040 GeneticVariation BEFREE Single nucleotide polymorphisms (SNPs) within the β(1)- (Ser49Gly, Arg389Gly) and β(2)-adrenoceptor (Arg16Gly, Gln27Glu, Thr164Ile) have been associated with alterations in adrenoceptor (AR) function sensitivity in vitro and in vivo and possibly contribute to HF progression. 20803192 2010
Heart failure
CUI: C0018801
Disease: Heart failure
0.040 GeneticVariation BEFREE Beta-2 adrenergic receptor gene polymorphisms Gln27Glu, Arg16Gly in patients with heart failure. 19886995 2009
Heart failure
CUI: C0018801
Disease: Heart failure
0.040 GeneticVariation BEFREE Arginine 16 glycine beta2-adrenoceptor polymorphism and cardiovascular structure and function in patients with heart failure. 17336757 2007