RS786204963 CDKL5
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What This Variant Does
"CLNSIG=4
Associated Conditions
Atypical Rett syndrome
Inborn genetic diseases
CDKL5 disorder
Developmental and epileptic encephalopathy
2
Angelman syndrome-like
Atypical Rett syndrome
Inborn genetic diseases
CDKL5 disorder
Developmental and epileptic encephalopathy
2
Angelman syndrome-like
Other Variants in CDKL5