RS797044912 CHD2

Health Risk Chr 15:93020140
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy 94
Seizure
Inborn genetic diseases
Developmental and epileptic encephalopathy 94
Seizure
Other Variants in CHD2
rs397514739 rs397514740 rs398122998 rs398122999 rs398123000 rs144667627 rs186163798 rs143043614 rs565686460 rs749969667
Ask Dr. Hemsworth about this variant