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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN1B
(E23K +1 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 5
GUncertain significance
SCN1B
(R56C +1 more)
Single nucleotide variant
(missense variant)
Generalized epilepsy with febrile seizures plus, type 1
+5 more
GConflicting classifications of pathogenicity