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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DIP2C
(R88W)
Single nucleotide variant
(missense variant)
Neurodevelopmental delay
+1 more
GUncertain significance
ADARB2, AKR1C1
+15 more
Copy number loss
Neurooculocardiogenitourinary syndrome
GPathogenic