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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD2
(I812T)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy 94
GLikely pathogenic
CHD2
(K1343fs)
Duplication
(frameshift variant)
Developmental and epileptic encephalopathy 94
GPathogenic