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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNB1
(R583*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 26
+1 more
GPathogenic/Likely pathogenic
KCNB1
(W369*)
Single nucleotide variant
(nonsense)
Intellectual disability
GPathogenic
KCNB1
(R312H)
Single nucleotide variant
(missense variant)
not provided
+7 more
GPathogenic/Likely pathogenic
KCNB1
(Q215*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
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