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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129993082, LOC129993083
+661 more
Copy number gain
See cases
GPathogenic
NUDT6
Single nucleotide variant
(intron variant)
not provided
GBenign
SCOC, SCRG1
+218 more
Copy number gain
See cases
GPathogenic
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