rs1799971, OPRM1

N. diseases: 95
Disease: Hypoalgesia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypoalgesia
CUI: C0085625
Disease: Hypoalgesia
0.010 GeneticVariation BEFREE In this study, we expanded on previous findings related to the 3 SNPs in the opioid receptor mu subunit (OPRM1 rs1799971), catechol-O-methyltransferase (COMT rs4680), and fatty acid amide hydrolase (FAAH rs324420) genes associated with placebo hypoalgesia and tested the effect of a 3-way interaction on placebo hypoalgesia. 31335650 2019