WASF1:Ensemblv115

WASP family member 1
OMIM: 605035, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green WASF1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Australian Genomics Health Alliance Epilepsy Flagship
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Neurodevelopmental disorder with absent language and variable seizures , MIM#618707