RS864309547 CHD2

Health Risk Chr 15:93020014
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy 94
Inborn genetic diseases
CHD2-related disorder
Developmental and epileptic encephalopathy 94
Inborn genetic diseases
CHD2-related disorder
Other Variants in CHD2
rs397514739 rs397514740 rs398122998 rs398122999 rs398123000 rs797044912 rs144667627 rs186163798 rs143043614 rs565686460
Ask Dr. Hemsworth about this variant