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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(P458A)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
GUncertain significance
FLNC
(R1762fs)
Deletion
(frameshift variant +1 more)
FLNC-associated cardiomyopathy
GLikely pathogenic