Gene entry
PRDM5
PR/SET domain 5
- Chromosome
- 4
- Cytoband
- 4q27
- Variants (rsID)
- 35
PRDM5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q27). Its official name is “PR/SET domain 5”. The reference table lists 35 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs343192Benignsingle nucleotide variantBrittle cornea syndrome 1
- rs185134294Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 2|Ehlers-Danlos syndrome
- rs77157999Conflicting interpretationssingle nucleotide variantBrittle cornea syndrome 1
- rs201325904Uncertain significancesingle nucleotide variantBrittle cornea syndrome 1
- rs201945549Uncertain 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.