Gene entry
COG1
component of oligomeric golgi complex 1
- Chromosome
- 17
- Cytoband
- 17q25.1
- Variants (rsID)
- 14
COG1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.1). Its official name is “component of oligomeric golgi complex 1”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1026128Benignsingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs117344829Benignsingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs142719529Benignsingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs144989249Benignsingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs3829571Benignsingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs117208167Conflicting interpretationssingle nucleotide variantCOG1 congenital disorder of glycosylation
- rs146066919Conflicting interpretationssingle nucleotide variantCOG1 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.