Gene entry
CYP4F22
cytochrome P450 family 4 subfamily F member 22
- Chromosome
- 19
- Cytoband
- 19p13.12
- Variants (rsID)
- 23
CYP4F22 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.12). Its official name is “cytochrome P450 family 4 subfamily F member 22”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs2280434Benignsingle nucleotide variantAutosomal recessive congenital ichthyosis 5
- rs73512652Benignsingle nucleotide variantAutosomal recessive congenital ichthyosis 5
- rs118203935Pathogenicsingle nucleotide variantAutosomal recessive congenital ichthyosis 5|Lamellar ichthyosis
- rs200464692Uncertain significancesingle nucleotide variantAutosomal recessive congenital ichthyosis 5
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.