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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNB2
(A323T +9 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CACNB2
Single nucleotide variant
(intron variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
CACNB2
(P516A +9 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 4
+2 more
GUncertain significance
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