RS587784440 SPTAN1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
5
Undetermined early-onset epileptic encephalopathy
Inborn genetic diseases
SPTAN1-related disorder
Early-infantile DEE
Focal epilepsy
See cases
Developmental and epileptic encephalopathy
5
Developmental delay with or without epilepsy
SPTAN1-related disorder
Early-infantile DEE
Developmental and epileptic encephalopathy
5
Other Variants in SPTAN1