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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN1B
(R125H +1 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GUncertain significance
SCN1B
(D120fs +1 more)
Indel
(frameshift variant)
Brugada syndrome 1
GUncertain significance