Gene entry
OTOA
otoancorin
- Chromosome
- 16
- Cytoband
- 16p12.2|16p12.2
- Variants (rsID)
- 14
OTOA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p12.2|16p12.2). Its official name is “otoancorin”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs138141474Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 22
- rs145160241Benignsingle nucleotide variantHearing loss, autosomal recessive
- rs148690740Pathogenicsingle nucleotide variantRare genetic deafness
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.