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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNB2
(A127V +4 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
CACNB2
(E507K +9 more)
Single nucleotide variant
(missense variant)
Brugada syndrome 4
+1 more
GUncertain significance