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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCND3
(T600I +1 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 9
+1 more
GUncertain significance
KCND3
(G380W)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
GLikely pathogenic