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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(L908V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GPathogenic
DNAAF3, TNNI3
+1 more
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 7
+9 more
GConflicting classifications of pathogenicity