RS796052621 KCNQ2

Health Risk Chr 20:63444756
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Inborn genetic diseases
Seizures
benign familial neonatal
1
Developmental and epileptic encephalopathy
7
See cases
Complex neurodevelopmental disorder
Early-infantile DEE
Early-infantile DEE
Inborn genetic diseases
Seizures
benign familial neonatal
1
Developmental and epileptic encephalopathy
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs74315391 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192218
Ask Dr. Hemsworth about this variant