Gene entry
SLC7A9
solute carrier family 7 member 9
- Chromosome
- 19
- Cytoband
- 19q13.11
- Variants (rsID)
- 17
SLC7A9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.11). Its official name is “solute carrier family 7 member 9”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1007160Benignsingle nucleotide variantCystinuria
- rs79389353Conflicting interpretationssingle nucleotide variantCystinuria
- rs121908480Pathogenicsingle nucleotide variantCystinuria
- rs121908482Pathogenicsingle nucleotide variantCystinuria
- rs121908484Pathogenicsingle nucleotide variantCystinuria
- rs121908486Pathogenicsingle nucleotide variantCystinuria
- rs745319034PathogenicDuplicationCystinuria
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.