PanelApp (staging)
  1. Genes and Genomic Entities
  2. CHRNB2

CHRNB2

cholinergic receptor nicotinic beta 2 subunit
OMIM: 118507, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green CHRNB2 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epilepsy, nocturnal frontal lobe, 3, MIM# 605375

Green CHRNB2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Epilepsy, nocturnal frontal lobe, 3, MIM# 605375