{{Rsnum
|rsid=324419
|Gene=FAAH
|Chromosome=1
|position=46406314
|Orientation=minus
|GMAF=0.08815
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 26.8 | 72.3
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 17.8 | 80.8
| ASW | 1.8 | 33.3 | 64.9
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 1.8 | 98.2
| GIH | 3.0 | 34.7 | 62.4
| LWK | 2.7 | 21.8 | 75.5
| MEX | 1.8 | 12.3 | 86.0
| MKK | 3.9 | 29.2 | 66.9
| TSI | 8.0 | 24.0 | 68.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20044928
|Title=Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity
|OA=1
}}

{{PMID Auto
|PMID=22473870
|Title=Contribution of genetic variants to pain susceptibility in Parkinson disease
}}

{{PMID Auto
|PMID=17991615
|Title=Rapid screening for potentially relevant polymorphisms in the human fatty acid amide hydrolase gene using Pyrosequencing.
}}

{{PMID Auto
|PMID=19014633
|Title=Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.
|OA=1
}}

{{PMID Auto
|PMID=20033240
|Title=Eating disorders: the current status of molecular genetic research.
|OA=1
}}

{{PMID Auto
|PMID=20054193
|Title=Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population.
}}

{{PMID Auto
|PMID=21423693
|Title=Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}