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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RYR2
(F1942C)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
RYR2
(I4554T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance