RS118192235 KCNQ2

Health Risk Chr 20:63413470 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Epileptic encephalopathy
Seizures
benign familial neonatal
1
Inborn genetic diseases
Complex neurodevelopmental disorder
Early-infantile DEE
Early-infantile DEE
Epileptic encephalopathy
Seizures
benign familial neonatal
1
Inborn genetic diseases
Complex neurodevelopmental disorder
Early-infantile DEE
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs74315391 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192218
Ask Dr. Hemsworth about this variant