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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PPP3CA
(A447T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
PPP3CA
(T387fs +1 more)
Duplication
(frameshift variant)
Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
+2 more
GPathogenic/Likely pathogenic