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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ1
(S27T)
Single nucleotide variant
(missense variant +1 more)
Atrial fibrillation, familial, 3
+3 more
GUncertain significance
KCNQ1
(A300E +2 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+5 more
GConflicting classifications of pathogenicity
KCNQ1
(R594Q +5 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia
+9 more
GPathogenic/Likely pathogenic
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