Gene entry
PHF6
PHD finger protein 6
- Chromosome
- X
- Cytoband
- Xq26.2
- Variants (rsID)
- 13
PHF6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq26.2). Its official name is “PHD finger protein 6”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs104894918Pathogenicsingle nucleotide variantBorjeson-Forssman-Lehmann syndrome
- rs132630297Pathogenicsingle nucleotide variantBorjeson-Forssman-Lehmann syndrome
- rs132630298Pathogenicsingle nucleotide variantBorjeson-Forssman-Lehmann syndrome
- rs132630299Pathogenicsingle nucleotide variantBorjeson-Forssman-Lehmann syndrome
- rs132630301Pathogenicsingle nucleotide variantBorjeson-Forssman-Lehmann syndrome
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.