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Gene entry

COG8

component of oligomeric golgi complex 8

Chromosome
16
Cytoband
16q22.1
Variants (rsID)
12

COG8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.1). Its official name is “component of oligomeric golgi complex 8”. The reference table lists 12 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs76253513Benignsingle nucleotide variantCOG8-congenital disorder of glycosylation
  • rs113642086Conflicting interpretationssingle nucleotide variantCOG8-congenital disorder of glycosylation
  • rs140736262Conflicting interpretationssingle nucleotide variantCOG8-congenital disorder of glycosylation
  • rs72795277Conflicting interpretationssingle nucleotide variantCOG8-congenital disorder of glycosylation
  • rs142169776Uncertain significancesingle nucleotide variantCOG8-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.