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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ2
(I278T)
Single nucleotide variant
(missense variant)
KCNQ2-related disorder
+3 more
GPathogenic/Likely pathogenic
KCNQ2
(R207W)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 7
+4 more
GPathogenic
KCNQ2
(C106G)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 7
GLikely pathogenic
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