Gene entry
PHF8
PHD finger protein 8
- Chromosome
- X
- Cytoband
- Xp11.22
- Variants (rsID)
- 8
PHF8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.22). Its official name is “PHD finger protein 8”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs148215758Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs121918523Pathogenicsingle nucleotide variantSyndromic X-linked intellectual disability Siderius type
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.
