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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL3
(E177G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 8
+5 more
GUncertain significance
MYL3
(R154C)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity