Gene entry
COG7
component of oligomeric golgi complex 7
- Chromosome
- 16
- Cytoband
- 16p12.2
- Variants (rsID)
- 18
COG7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p12.2). Its official name is “component of oligomeric golgi complex 7”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs16940094Benignsingle nucleotide variantCOG7 congenital disorder of glycosylation
- rs114458562Conflicting interpretationssingle nucleotide variantCOG7 congenital disorder of glycosylation
- rs142744907Conflicting interpretationssingle nucleotide variantCOG7 congenital disorder of glycosylation
- rs144814374Conflicting interpretationssingle nucleotide variantCOG7 congenital disorder of glycosylation
- rs149481813Conflicting interpretationssingle nucleotide variantCOG7 congenital disorder of glycosylation
- rs150104389Conflicting interpretationsDeletionCongenital disorder of glycosylation|COG7 congenital disorder of glycosylation
- rs146918812Uncertain significancesingle nucleotide variantCOG7 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.