RS796053138 SCN2A

Health Risk Chr 2:165377645
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Intellectual disability
SCN2A-related disorder
Inborn genetic diseases
Seizure
Complex neurodevelopmental disorder
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687
Ask Dr. Hemsworth about this variant