SNRPN

small nuclear ribonucleoprotein polypeptide N
OMIM: 182279, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SNRPN in Paediatric motor neuronopathies


Level 2: Neurology
Version 3.12
Latest signed off version: v3.9 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review Other - please specifiy in evaluation comments
    Sources
    • Expert Review Red
    • Emory Genetics Laboratory
    Phenotypes
    • Prader-Willi syndrome, OMIM:176270
    Tags
    • currently-ngs-unreportable