RS796053137 SCN2A

Health Risk Chr 2:165377606
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What This Variant Does
"rs796053137, also known as c.4264A&gt
Associated Conditions
Complex neurodevelopmental disorder
Benign familial neonatal-infantile seizures 1
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
SCN2A-related generalized epilepsy with febrile seizures plus
Complex neurodevelopmental disorder
Benign familial neonatal-infantile seizures 1
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687
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