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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC
(R1159G)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 5
+4 more
GUncertain significance
FLNC, FLNC-AS1
(G2088R +1 more)
Single nucleotide variant
(missense variant)
Myofibrillar myopathy 5
GUncertain significance