Gene entry
DEAF1
DEAF1 transcription factor
- Chromosome
- 11
- Cytoband
- 11p15.5
- Variants (rsID)
- 16
DEAF1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.5). Its official name is “DEAF1 transcription factor”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs10615Benignsingle nucleotide variant
- rs1057518811Conflicting interpretationssingle nucleotide variant9 conditions|Intellectual disability-epilepsy-extrapyramidal 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.