RS796052631 KCNQ2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
KCNQ2-related disorder
Early-infantile DEE
Developmental and epileptic encephalopathy
7
Inborn genetic diseases
KCNQ2-related disorder
Early-infantile DEE
Developmental and epileptic encephalopathy
7
Other Variants in KCNQ2