MIR96

microRNA 96
OMIM: 611606, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber MIR96 in Monogenic hearing loss


Level 2: Audiology
Version 6.16
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Expert
    • UKGTN
    Phenotypes
    • Deafness, autosomal dominant 50 613074
    Tags
    • locus-type-rna-micro