Gene entry
SLC20A2
solute carrier family 20 member 2
- Chromosome
- 8
- Cytoband
- 8p11.21
- Variants (rsID)
- 19
SLC20A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p11.21). Its official name is “solute carrier family 20 member 2”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs3763510Benignsingle nucleotide variantIdiopathic basal ganglia calcification 1
- rs79577461Benignsingle nucleotide variantIdiopathic basal ganglia calcification 1
- rs398122395PathogenicDeletionIdiopathic basal ganglia calcification 1
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.