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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
Deletion
(inframe_deletion)
Long QT syndrome 3
+3 more
GPathogenic
SCN5A
(E462K)
Single nucleotide variant
(missense variant)
Brugada syndrome 1
+10 more
GUncertain significance