RS794727152 SCN2A

Health Risk Chr 2:165342465
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What This Variant Does
"rs794727152, also known as c.2558G&gt
Associated Conditions
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Complex neurodevelopmental disorder
West syndrome
Seizures
benign familial infantile
3
Developmental and epileptic encephalopathy
11
Developmental and epileptic encephalopathy
11
Seizures
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687
Ask Dr. Hemsworth about this variant