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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN1B
(G178V)
Single nucleotide variant
(intron variant +1 more)
Brugada syndrome 5
GUncertain significance
SCN1B
(R191Q)
Single nucleotide variant
(missense variant +1 more)
Generalized epilepsy with febrile seizures plus, type 1
+1 more
GUncertain significance