SS18L1

SS18L1, nBAF chromatin remodeling complex subunit
OMIM: 606472, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SS18L1 in Adult onset neurodegenerative disorder


Level 2: Neurology
Version 8.11
Latest signed off version: v8.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
  • Yorkshire and North East GLH
Phenotypes
  • Amyotrophic lateral sclerosis, MONDO:0004976
Tags
  • gene-checked