FAAH, fatty acid amide hydrolase, 2166

N. diseases: 177; N. variants: 8
Disease: Drug abuse ×
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: C0013146
Disease:
Drug abuse 		0.010 GeneticVariation BEFREE The human fatty acid amide hydrolase (FAAH) missense mutation c.385 C-->A, which results in conversion of a conserved proline residue to threonine (P129T), has been associated with street drug use and problem drug abuse. 16972078 2006