Gene entry
SLC25A20
solute carrier family 25 member 20
- Chromosome
- 3
- Cytoband
- 3p21.31
- Variants (rsID)
- 7
SLC25A20 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.31). Its official name is “solute carrier family 25 member 20”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs542582794Likely benignsingle nucleotide variantCarnitine acylcarnitine translocase deficiency
- rs541208710Pathogenicsingle nucleotide variantCarnitine acylcarnitine translocase deficiency
- rs757552268PathogenicDeletionCarnitine acylcarnitine translocase deficiency
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.