RS796053124 SCN2A

Health Risk Chr 2:165354232
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
11
Seizure
Hereditary episodic ataxia
Vertigo
Inborn genetic diseases
SCN2A-related disorder
Developmental and epileptic encephalopathy
11
Seizure
Hereditary episodic ataxia
Vertigo
Inborn genetic diseases
SCN2A-related disorder
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687
Ask Dr. Hemsworth about this variant