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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO18B
(R2220fs +1 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
MYO18B
(L2257fs +1 more)
Deletion
(frameshift variant)
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
GLikely pathogenic