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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RBM20
(P706T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
RBM20
(A778V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
RBM20
(E1173K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1DD
+2 more
GUncertain significance
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