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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LINC01708, LINC01709
+549 more
Copy number gain
See cases
GPathogenic
CNN3, CNN3-DT
+1 more
(V16I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance