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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNQ1
(A341V +3 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GPathogenic
KCNQ1
(Q565P +4 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 1
+1 more
GUncertain significance