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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935726, LOC129935727
+1665 more
Copy number gain
See cases
GPathogenic
CUL3, LOC129935709
(K6R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance