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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.