Gene entry
RUNX2
RUNX family transcription factor 2
- Chromosome
- 6
- Cytoband
- 6p21.1
- Variants (rsID)
- 33
RUNX2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.1). Its official name is “RUNX family transcription factor 2”. The reference table lists 33 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs11498198Benignsingle nucleotide variantCleidocranial dysostosis
- rs147359883Conflicting interpretationssingle nucleotide variant
- rs104893989Pathogenicsingle nucleotide variantCleidocranial dysostosis
- rs104893995Pathogenicsingle nucleotide variantCleidocranial dysostosis
- rs864621970Pathogenicsingle nucleotide variantCleidocranial dysostosis
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.
