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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNB1
(V413I)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 26
GPathogenic/Likely pathogenic
KCNB1
(W369L)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 26
GPathogenic/Likely pathogenic