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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH2
(S681fs +1 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
KCNH2
(P628fs +1 more)
Duplication
(frameshift variant)
Long QT syndrome
+1 more
GPathogenic
KCNH2
(Q335* +3 more)
Single nucleotide variant
(nonsense)
Long QT syndrome
GPathogenic
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