RS398122998 CHD2

Health Risk Chr 15:93020076
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy 94
Inborn genetic diseases
Developmental and epileptic encephalopathy 94
Inborn genetic diseases
Other Variants in CHD2
rs397514739 rs397514740 rs398122999 rs398123000 rs797044912 rs144667627 rs186163798 rs143043614 rs565686460 rs749969667
Ask Dr. Hemsworth about this variant