Gene entry
SLC35A3
solute carrier family 35 member A3
- Chromosome
- 1
- Cytoband
- 1p21.2
- Variants (rsID)
- 10
SLC35A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p21.2). Its official name is “solute carrier family 35 member A3”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs141952252Pathogenicsingle nucleotide variantAutism spectrum disorder - epilepsy - arthrogryposis syndrome
- rs398122524Pathogenicsingle nucleotide variantAutism spectrum disorder - epilepsy - arthrogryposis 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.