Gene entry
SLC25A12
solute carrier family 25 member 12
- Chromosome
- 2
- Cytoband
- 2q31.1
- Variants (rsID)
- 19
SLC25A12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q31.1). Its official name is “solute carrier family 25 member 12”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs142179562Benignsingle nucleotide variant
- rs149278617Benignsingle nucleotide variant
- rs35565687Benignsingle nucleotide variant
- rs35881803Benignsingle nucleotide variant
- rs3765166Benignsingle nucleotide variant
- rs121434396Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 39
- rs138477378Uncertain significancesingle nucleotide 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.