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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(E1220del)
Deletion
(inframe_deletion)
Ebstein anomaly
GUncertain significance
MYH7
(Q1160H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+1 more
GUncertain significance