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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADO, ANK3
+227 more
Copy number gain
See cases
GPathogenic
LOC129390190, LOC129390191
+610 more
Copy number loss
See cases
GPathogenic
BICC1, LOC126860938
Single nucleotide variant
(intron variant)
not provided
GLikely benign
BICC1, LOC126860938
(V747A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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