RS587776935 AKT3
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
Polymicrogyria
Capillary hemangioma
Global developmental delay
Macrocephaly
Inborn genetic diseases
See cases
Neoplasm
AKT3-related disorder
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
Polymicrogyria
Capillary hemangioma
Global developmental delay
Macrocephaly
Inborn genetic diseases
Other Variants in AKT3