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Gene entry

FAAH

fatty acid amide hydrolase

Chromosome
1
Cytoband
1p33
Variants (rsID)
17

FAAH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p33). Its official name is “fatty acid amide hydrolase”. The reference table lists 17 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs324420Benignsingle nucleotide variantFAAH POLYMORPHISM
  • rs324419Not classifiedsynonymous_variantBody Mass Index Quantitative Trait Locus 11|Parkinson Disease, Late-Onset

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.