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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL2
(M69L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
GUncertain significance
MYL2
(N47K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+7 more
GConflicting classifications of pathogenicity