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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC110121269, SCN5A
(S1102F +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+10 more
GUncertain significance
LOC110121269, SCN5A
(Q1097K +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC110121269, SCN5A
(E1053K)
Single nucleotide variant
(missense variant)
Long QT syndrome 3
+5 more
GConflicting classifications of pathogenicity
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