Gene entry
ZNF335
zinc finger protein 335
- Chromosome
- 20
- Cytoband
- 20q13.12
- Variants (rsID)
- 15
ZNF335 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.12). Its official name is “zinc finger protein 335”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs116247914Benignsingle nucleotide variant
- rs16990964Benignsingle nucleotide variantMicrocephalic primordial dwarfism due to ZNF335 deficiency
- rs3746504Benignsingle nucleotide variantMicrocephalic primordial dwarfism due to ZNF335 deficiency
- rs3746512Benignsingle nucleotide variantMicrocephalic primordial dwarfism due to ZNF335 deficiency
- rs41305805Benignsingle nucleotide variantMicrocephalic primordial dwarfism due to ZNF335 deficiency
- rs117132825Conflicting interpretationssingle nucleotide variant
- rs190178539Conflicting interpretationssingle 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.