AVPR1A, arginine vasopressin receptor 1A, 552

N. diseases: 51; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030193
Disease: Pain
Pain
0.030 GeneticVariation phenotype BEFREE In patients with SCD, clinical factors such as pain and stress have been associated with increased health care utilization, but it is not known if the presence of the AVPR1A SNP plays a role in this observation. 31710639 2019
CUI: C0030193
Disease: Pain
Pain
0.030 GeneticVariation phenotype BEFREE Aim/Design: The purpose of this literature review was to describe mechanisms of the polymorphic gene AVPR1A and the phenotypic variations associated with its SNPs relative to health conditions and pain. 29503216 2018
CUI: C0030193
Disease: Pain
Pain
0.030 GeneticVariation phenotype BEFREE A genetic association study in humans revealed the influence of a single nucleotide polymorphism (rs10877969) in AVPR1A on capsaicin pain levels, but only in male subjects reporting stress at the time of testing. 22019732 2011