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Gene entry

COG5

component of oligomeric golgi complex 5

Chromosome
7
Cytoband
7q22.3
Variants (rsID)
51

COG5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q22.3). Its official name is “component of oligomeric golgi complex 5”. The reference table lists 51 variants (rsID) for this gene.

Clinically classified variants

14 reference-table entries with clinical significance.

  • rs116603307Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs184902233Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs2269970Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs35581984Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs73419464Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs74443110Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs74522314Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs79413133Benignsingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs113660545Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs142433421Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs142970891Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs189560910Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs35393416Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation
  • rs41276187Conflicting interpretationssingle nucleotide variantCOG5-congenital disorder of glycosylation

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.