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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA2
(L341P)
Single nucleotide variant
(intron variant +1 more)
Developmental and epileptic encephalopathy, 32
+1 more
GUncertain significance
KCNA2
(H196fs)
Duplication
(frameshift variant)
Developmental and epileptic encephalopathy, 32
GLikely pathogenic
KCNA2
(P161fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
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