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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNB2
Single nucleotide variant
(splice donor variant +1 more)
not provided
GUncertain significance
CACNB2
(T449I +9 more)
Single nucleotide variant
(missense variant)
Ventricular tachycardia
+5 more
GConflicting classifications of pathogenicity
ARL5B, LARP4B
+180 more
Copy number gain
Mosaic supernumerary isodicentric chromosome 10
Gnot provided
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