Gene entry
CHCHD10
coiled-coil-helix-coiled-coil-helix domain containing 10
- Chromosome
- 22
- Cytoband
- 22q11.23
- Variants (rsID)
- 2
CHCHD10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q11.23). Its official name is “coiled-coil-helix-coiled-coil-helix domain containing 10”. The reference table lists 2 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs131444Benignsingle nucleotide variantAutosomal dominant mitochondrial myopathy with exercise intolerance|Lower motor neuron syndrome with late-adult onset|Frontotemporal dementia and/or amyotrophic lateral sclerosis 2|Lower motor neuron syndrome with late-adult onset|Frontotemporal dementia and/or amyotrophic lateral sclerosis 2|Autosomal dominant mitochondrial myopathy with exercise intolerance
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.