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Gene entry

CHD9

chromodomain helicase DNA binding protein 9

Chromosome
16
Cytoband
16q12.2
Variants (rsID)
39

CHD9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q12.2). Its official name is “chromodomain helicase DNA binding protein 9”. The reference table lists 39 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs3743771Not classifiedmissense_variantMissense_T2254A
  • rs6499548Not classifiedmissense_variantMissense_D1806E

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.