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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LDB3
(R31W)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+5 more
GUncertain significance
LDB3
(R218H +2 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
LDB3
(P404A +4 more)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 4
+1 more
GUncertain significance
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