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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ1, KCNQ1OT1
(L316fs +4 more)
Deletion
(frameshift variant)
Long QT syndrome 1
GLikely pathogenic
KCNQ1OT1, KCNQ1
Deletion
Long QT syndrome 1
GPathogenic