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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ1
(G118fs +1 more)
Deletion
(frameshift variant)
Abnormality of the cardiovascular system
GPathogenic
KCNQ1
(F296fs +1 more)
Duplication
(frameshift variant)
Atrial fibrillation, familial, 3
+9 more
GPathogenic/Likely pathogenic
KCNQ1
(R555H +4 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia
+8 more
GPathogenic/Likely pathogenic
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