Gene entry
SLC30A10
solute carrier family 30 member 10
- Chromosome
- 1
- Cytoband
- 1q41
- Variants (rsID)
- 13
SLC30A10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q41). Its official name is “solute carrier family 30 member 10”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs281860284Pathogenicsingle nucleotide variantHypermanganesemia with dystonia, polycythemia, and cirrhosis
- rs281860288PathogenicDeletionHypermanganesemia with dystonia, polycythemia, and cirrhosis
- rs281860292PathogenicDeletionHypermanganesemia with dystonia, polycythemia, and cirrhosis
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.