Gene entry
SLC39A13
solute carrier family 39 member 13
- Chromosome
- 11
- Cytoband
- 11p11.2
- Variants (rsID)
- 3
SLC39A13 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p11.2). Its official name is “solute carrier family 39 member 13”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs35741412Benignsingle nucleotide variantEhlers-Danlos syndrome, spondylocheirodysplastic type|Ehlers-Danlos syndrome|Connective tissue disorder
- rs140574574Conflicting interpretationssingle nucleotide variant6 conditions|Ehlers-Danlos syndrome, spondylocheirodysplastic type|Connective tissue disorder|Ehlers-Danlos syndrome
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.