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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYN1
(I384V)
Single nucleotide variant
(missense variant)
Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders
GUncertain significance
SYN1
Single nucleotide variant
(splice acceptor variant)
SYN1-related disorder
+1 more
GLikely pathogenic