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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEK9
(P769T +2 more)
Inversion
(missense variant)
not provided
GUncertain significance
NEK9
(L104fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
NEK9
(Y69*)
Single nucleotide variant
(nonsense +1 more)
not provided
GLikely pathogenic
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