Genetics University — Research, Education, Medical Genetics
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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.