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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASCC3, CCNC
+68 more
Copy number loss
See cases
GPathogenic
ASCC3, CCNC
+53 more
Copy number loss
See cases
GPathogenic
FBXL4, LOC129996867
Deletion
(intron variant)
not provided
GBenign
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