RS1064795618 EEF1A2

Health Risk Chr 20:63497693
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What This Variant Does
"CLNSIG=4
Associated Conditions
Intellectual disability
autosomal dominant 38
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
EEF1A2-related disorder
Intellectual disability
autosomal dominant 38
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
EEF1A2-related disorder
Other Variants in EEF1A2
rs587777162 rs786205865 rs786205866 rs879255373 rs886039346 rs886042041 rs886041197 rs1057518587 rs1057521655 rs1131691663
Ask Dr. Hemsworth about this variant