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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(E1784K +5 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 3
+7 more
GPathogenic/Likely pathogenic
SCN5A
(R282C)
Single nucleotide variant
(missense variant)
Brugada syndrome 1
+3 more
GConflicting classifications of pathogenicity