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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRK5, GRK5-IT1
+1 more
(V11F)
Indel
(missense variant)
Neurodevelopmental disorder
GUncertain significance
CACUL1, PLPP4
+22 more
Copy number loss
Astigmatism
+4 more
GUncertain significance