RS879255373 EEF1A2

Health Risk Chr 20:63488307
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What This Variant Does
"CLNSIG=4
Associated Conditions
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
Developmental and epileptic encephalopathy
33
Inborn genetic diseases
Other Variants in EEF1A2
rs587777162 rs786205865 rs786205866 rs886039346 rs886042041 rs886041197 rs1057518587 rs1057521655 rs1064795618 rs1131691663
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