Gene entry
SLC25A26
solute carrier family 25 member 26
- Chromosome
- 3
- Cytoband
- 3p14.1
- Variants (rsID)
- 39
SLC25A26 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p14.1). Its official name is “solute carrier family 25 member 26”. The reference table lists 39 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs13874Benignsingle nucleotide variantCombined oxidative phosphorylation deficiency 28
- rs146159281Benignsingle nucleotide variantCombined oxidative phosphorylation deficiency 28
- rs2311298Benignsingle nucleotide variant
- rs3772197Benignsingle nucleotide variant
Other listed variants
- rs332341
- rs782728
- rs782733
- rs782744
- rs1046844
- rs4443106
- rs6777571
- rs7651232
- rs9827734
- rs17044348
- rs28367017
- rs28534383
- rs28602282
- rs36129553
- rs36149310
- rs76584352
- rs77017807
- rs78008713
- rs79705855
- rs114718969
- rs114953780
- rs116392630
- rs118053447
- rs138327553
- rs139695822
- rs142010930
- rs143948684
- rs145318622
- rs147368461
- rs147781870
- rs148689258
- rs149478945
- rs150159218
- rs192926084
- rs202218035
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.