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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(R1341*)
Single nucleotide variant
(nonsense)
Primary familial dilated cardiomyopathy
+7 more
GPathogenic/Likely pathogenic
FLNC, FLNC-AS1
(Q1802* +1 more)
Single nucleotide variant
(nonsense)
Primary familial dilated cardiomyopathy
+1 more
GPathogenic/Likely pathogenic
FLNC, FLNC-AS1
(G2118S +1 more)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 5
+5 more
GConflicting classifications of pathogenicity
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