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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(A193T)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
FLNC
(P679L)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
FLNC
(W1766R)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+6 more
GUncertain significance
FLNC, FLNC-AS1
(V2614fs +1 more)
Microsatellite
(frameshift variant)
Dilated Cardiomyopathy, Dominant
+4 more
GPathogenic/Likely pathogenic
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