Gene entry
CLCN7
Cl-/H+ antiporter 7
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 15
CLCN7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “Cl-/H+ antiporter 7”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs117183989Benignsingle nucleotide variantOsteopetrosis|Increased bone mineral density
- rs387907576Pathogenicsingle nucleotide variantAutosomal dominant osteopetrosis 2|Autosomal recessive osteopetrosis 4
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.