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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC115, CCDC74B
+19 more
Copy number loss
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies
GPathogenic
MZT2B, TUBA3E
(A426E)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
GUncertain significance