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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(I852F)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
GUncertain significance
FLNC
(F1371C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
GUncertain significance
FLNC
(K1530Q)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
GUncertain significance
FLNC, FLNC-AS1
(D2510H +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
GUncertain significance
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