RS587777162 EEF1A2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
Intellectual disability
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy
autosomal dominant 38
EEF1A2-related disorder
Complex neurodevelopmental disorder
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
Intellectual disability
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy
autosomal dominant 38
EEF1A2-related disorder
Other Variants in EEF1A2