Gene entry
FAM20A
FAM20A golgi associated secretory pathway pseudokinase
- Chromosome
- 17
- Cytoband
- 17q24.2
- Variants (rsID)
- 19
FAM20A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q24.2). Its official name is “FAM20A golgi associated secretory pathway pseudokinase”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2302234Benignsingle nucleotide variantAmelogenesis imperfecta type 1G
- rs2907373Benignsingle nucleotide variantAmelogenesis imperfecta type 1G
- rs200599944Uncertain significancesingle nucleotide variant
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.