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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(E1784K +5 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GPathogenic/Likely pathogenic
KCNQ1
(F339Y +3 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 1
+1 more
GConflicting classifications of pathogenicity
KCNQ1
(F339S +3 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
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