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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKL5
(Q791P)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 2
+5 more
GBenign
CDKL5, RS1
(I194fs)
Deletion
(frameshift variant +1 more)
Retinal dystrophy
+2 more
GPathogenic