Gene entry
SLC26A5
solute carrier family 26 member 5
- Chromosome
- 7
- Cytoband
- 7q22.1
- Variants (rsID)
- 21
SLC26A5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q22.1). Its official name is “solute carrier family 26 member 5”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs116900495Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 61
- rs117444825Benignsingle nucleotide variant
- rs141436712Benignsingle nucleotide variant
- rs141952919Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 61
- rs148546326Conflicting interpretationssingle nucleotide variant
- rs146547672Likely benignsingle nucleotide variant
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.