Gene entry
FASN
fatty acid synthase
- Chromosome
- 17
- Cytoband
- 17q25.3
- Variants (rsID)
- 15
FASN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.3). Its official name is “fatty acid synthase”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs12946178Benignsingle nucleotide variantEpileptic encephalopathy
- rs145688025Benignsingle nucleotide variantEpileptic encephalopathy
- rs150748779Benignsingle nucleotide variantEpileptic encephalopathy
- rs2229426Benignsingle nucleotide variantEpileptic encephalopathy
- rs199546508Uncertain significancesingle nucleotide variantEpileptic encephalopathy
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.
