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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ2
(V710fs +3 more)
Deletion
(frameshift variant)
not provided
+2 more
GPathogenic
KCNQ2
(R541T +3 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GConflicting classifications of pathogenicity
KCNQ2
(G313R)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 7
+2 more
GPathogenic/Likely pathogenic
KCNQ2
(G281R)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GPathogenic/Likely pathogenic
KCNQ2
(T274M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
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