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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOL3
(P87T +2 more)
Single nucleotide variant
(missense variant)
Myoclonus, familial, 1
GUncertain significance
ACD, AGRP
+47 more
Copy number loss
not provided
GPathogenic