Gene entry
SLC17A8
solute carrier family 17 member 8
- Chromosome
- 12
- Cytoband
- 12q23.1
- Variants (rsID)
- 19
SLC17A8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q23.1). Its official name is “solute carrier family 17 member 8”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs138307707Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 25
- rs121918339Likely pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 25
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.