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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111B
(C458fs +1 more)
Deletion
(frameshift variant)
Myositis disease
+4 more
GLikely pathogenic
FKBP10
(G278fs)
Duplication
(frameshift variant)
Abnormality of the skeletal system
+6 more
GConflicting classifications of pathogenicity