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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKAP9, LOC121175350
(R1679C)
Single nucleotide variant
(missense variant)
Long QT syndrome
+2 more
GUncertain significance
AKAP9
(E2147Q +1 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+1 more
GUncertain significance