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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH2
(G1087fs +2 more)
Insertion
(frameshift variant +1 more)
Long QT syndrome 2
GLikely pathogenic
KCNH2
(Y135* +4 more)
Single nucleotide variant
(nonsense)
Long QT syndrome 2
GPathogenic