MIR96

microRNA 96
OMIM: 611606, Gene2Phenotype

1 panel

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

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.39
Latest signed off version: v4.0 (22 Mar 2023)

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