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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DES
(R227C)
Single nucleotide variant
(missense variant)
Desmin-related myofibrillar myopathy
+2 more
GUncertain significance
DES
(E283del +4 more)
Microsatellite
(inframe_deletion +1 more)
Dilated cardiomyopathy 1I
+2 more
GUncertain significance