FAAH, fatty acid amide hydrolase, 2166

N. diseases: 177; N. variants: 8
Disease: Hypoalgesia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs324420
rs324420
Entrez Id: 2166
Gene Symbol: FAAH
FAAH
CUI: C0085625
Disease:
Hypoalgesia 		0.010 GeneticVariation BEFREE OPRM1 rs1799971, COMT rs4680, and FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia. 31335650 2019