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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STXBP1
(R235G +2 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+2 more
GConflicting classifications of pathogenicity
STXBP1
(T476fs +3 more)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy, 4
GLikely pathogenic