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Gene entry

COMP

cartilage oligomeric matrix protein

Chromosome
19
Cytoband
19p13.11
Variants (rsID)
6

COMP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.11). Its official name is “cartilage oligomeric matrix protein”. The reference table lists 6 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

  • rs115338183Benignsingle nucleotide variantPseudoachondroplastic spondyloepiphyseal dysplasia syndrome|Multiple epiphyseal dysplasia type 1|Connective tissue disorder
  • rs61739916Benignsingle nucleotide variantPseudoachondroplastic spondyloepiphyseal dysplasia syndrome|Multiple epiphyseal dysplasia type 1|Connective tissue disorder
  • rs312262901Likely pathogenicsingle nucleotide variantPseudoachondroplastic spondyloepiphyseal dysplasia 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.