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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP43
(A277P +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
CEP43, MPC1
+2 more
Duplication
not provided
GUncertain significance
CEP43, RNASET2
Deletion
not provided
GPathogenic
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