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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(K1934Q +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
+2 more
GUncertain significance
SCN3A
(S1061A +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
GUncertain significance
SCN3A
(P614A)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
+1 more
GConflicting classifications of pathogenicity
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