RS121918321 STXBP1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Developmental and epileptic encephalopathy
4
Infantile epilepsy syndrome
Inborn genetic diseases
Early-infantile DEE
Developmental and epileptic encephalopathy
4
Infantile epilepsy syndrome
Inborn genetic diseases
Early-infantile DEE
Other Variants in STXBP1