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Gene entry

COG2

component of oligomeric golgi complex 2

Chromosome
1
Cytoband
1q42.2
Variants (rsID)
21

COG2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q42.2). Its official name is “component of oligomeric golgi complex 2”. The reference table lists 21 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs151309110Uncertain significancesingle nucleotide variantCongenital disorder of glycosylation, type IIq

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.