RASA2

RAS p21 protein activator 2
OMIM: 601589, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red RASA2 in Macrocephaly_Megalencephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.140

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Amber RASA2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services

Amber RASA2 in Rasopathy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.105

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Rasopathy

Amber RASA2 in Cardiomyopathy_Paediatric


Level 2: Cardiovascular disorders
Version 0.192

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • London South GLH
  • NHS GMS
Phenotypes
  • Noonan syndrome?

Amber RASA2 in Fetal anomalies


Version 1.255

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Noonan syndrome