1. Genes and Genomic Entities
  2. SNW1

SNW1

SNW domain containing 1
OMIM: 603055, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber SNW1 in Severe microcephaly


Level 2: Neurology
Version 9.11
Latest signed off version: v9.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • neurodevelopmental disorder, MONDO:0700092
  • microcephaly, MONDO:0001149
Tags
  • Q3_26_promote_green
Amber SNW1 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 9.40
Latest signed off version: v9.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    • microcephaly, MONDO:0001149
    Tags
    • Q3_26_promote_green
    Amber SNW1 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.60
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    • microcephaly, MONDO:0001149
    Tags
    • Q3_26_promote_green