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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DES
(S13F)
Single nucleotide variant
(missense variant)
Desmin-related myofibrillar myopathy
+2 more
GPathogenic
DES
(S72R)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
DES
(D213Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Desmin-related myofibrillar myopathy
GUncertain significance
DES
(E283del +4 more)
Microsatellite
(inframe_deletion +1 more)
Dilated cardiomyopathy 1I
+2 more
GUncertain significance
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