Genetics University — Research, Education, Medical Genetics
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Gene entry

OTOGL

otogelin like

Chromosome
12
Cytoband
12q21.31
Variants (rsID)
66

OTOGL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q21.31). Its official name is “otogelin like”. The reference table lists 66 variants (rsID) for this gene.

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Clinically classified variants

15 reference-table entries with clinical significance.

  • rs10862089Benignsingle nucleotide variant
  • rs11114416Benignsingle nucleotide variant
  • rs12304169Benignsingle nucleotide variant
  • rs141867785Benignsingle nucleotide variant
  • rs148064564Benignsingle nucleotide variant
  • rs1551122Benignsingle nucleotide variant
  • rs61729710Benignsingle nucleotide variant
  • rs61735664Benignsingle nucleotide variant
  • rs76420383Benignsingle nucleotide variant
  • rs77835094Benignsingle nucleotide variant
  • rs183159689Conflicting interpretationssingle nucleotide variantHearing impairment
  • rs188793584Conflicting interpretationssingle nucleotide variant
  • rs192234924Conflicting interpretationssingle nucleotide variant
  • rs192944055Conflicting interpretationssingle nucleotide variant
  • rs191608225Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 84B

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.