Genetics University — Research, Education, Medical Genetics
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Gene entry

CCDC22

CCC complex scaffolding subunit CCDC22

Chromosome
X
Cytoband
Xp11.23
Variants (rsID)
12

CCDC22 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.23). Its official name is “CCC complex scaffolding subunit CCDC22”. The reference table lists 12 variants (rsID) for this gene.

Clinically classified variants

5 reference-table entries with clinical significance.

  • rs113045747Benignsingle nucleotide variant
  • rs144632022Benignsingle nucleotide variantRitscher-Schinzel syndrome 2
  • rs147222955Benignsingle nucleotide variant
  • rs2294021Benignsingle nucleotide variantRitscher-Schinzel syndrome 2
  • rs143790434Conflicting 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.