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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYFIP2
(V525L +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 65
GLikely pathogenic
CYFIP2
(E665K +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability
+1 more
GPathogenic