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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCND3
(H476R)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
KCND3
(S162L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance