Gene entry
COQ9
coenzyme Q9
- Chromosome
- 16
- Cytoband
- 16q21
- Variants (rsID)
- 12
COQ9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q21). Its official name is “coenzyme Q9”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs115677652Benignsingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs223864Benignsingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs61730662Benignsingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs75908124Benignsingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs78846023Benignsingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs11547480Conflicting interpretationssingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs143587648Conflicting interpretationssingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs181356497Conflicting interpretationssingle nucleotide variantEncephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
- rs191446011Uncertain significancesingle nucleotide variant
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.