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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(S1776G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GUncertain significance
MYH7
(I263fs)
Deletion
(frameshift variant)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance