Gene entry
SLC35C1
solute carrier family 35 member C1
- Chromosome
- 11
- Cytoband
- 11p11.2
- Variants (rsID)
- 3
SLC35C1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p11.2). Its official name is “solute carrier family 35 member C1”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs10838518Benignsingle nucleotide variantLeukocyte adhesion deficiency type II
- rs141379070Conflicting interpretationssingle nucleotide variantLeukocyte adhesion deficiency type II
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.