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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PPP3CA
(A421S +2 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
GPathogenic
PPP3CA
(E282K)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
+4 more
GPathogenic/Likely pathogenic