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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCDH19
(P561S)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 9
GPathogenic
DIAPH2, FAM133A
+6 more
Deletion
Developmental and epileptic encephalopathy, 9
GPathogenic