Gene entry
SLC35A1
solute carrier family 35 member A1
- Chromosome
- 6
- Cytoband
- 6q15
- Variants (rsID)
- 12
SLC35A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q15). Its official name is “solute carrier family 35 member A1”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs114156788Benignsingle nucleotide variantSLC35A1-congenital disorder of glycosylation
- rs145006535Conflicting interpretationssingle nucleotide variantSLC35A1-congenital disorder of glycosylation
- rs149903512Conflicting interpretationssingle nucleotide variantSLC35A1-congenital disorder of glycosylation
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.