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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DENND5A, DNHD1
+723 more
Copy number gain
See cases
GPathogenic
ANO9, AP2A2
+266 more
Copy number gain
See cases
GPathogenic
DRD4
Indel
(missense variant)
not provided
GUncertain significance
CDHR5, DEAF1
+12 more
Copy number gain
See cases
GUncertain significance
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