rs77041280, HRH4

N. diseases: 2
Disease: Aortic Valve Insufficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Aortic Valve Insufficiency
CUI: C0003504
Disease: Aortic Valve Insufficiency
0.010 GeneticVariation BEFREE AR patients with mutant genotype (TA + AA) of rs77485247 and AR patients with mutant genotype (AT + TT) of rs77041280 had higher specific IgE, ECP levels, and VAS scores after treatment and lower incidence of adverse reactions and total effective rate than those with TT genotype and those with AA genotype, respectively. 27888642 2017