Gene entry
SLC11A2
solute carrier family 11 member 2
- Chromosome
- 12
- Cytoband
- 12q13.12
- Variants (rsID)
- 21
SLC11A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.12). Its official name is “solute carrier family 11 member 2”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs115874705Benignsingle nucleotide variantMicrocytic anemia with liver iron overload
- rs149411Benignsingle nucleotide variantMicrocytic anemia with liver iron overload
- rs121918367Pathogenicsingle nucleotide variantMicrocytic anemia with liver iron overload
- rs445520Not classifiedmissense_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.