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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNI3
(R192C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+6 more
GPathogenic/Likely pathogenic
TNNI3
(R162W)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 7
+7 more
GConflicting classifications of pathogenicity