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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLK4
(N59S +1 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly and chorioretinopathy 2
GUncertain significance
PLK4
(K277R +2 more)
Single nucleotide variant
(missense variant)
Microcephaly and chorioretinopathy 2
+2 more
GConflicting classifications of pathogenicity
PLK4
Single nucleotide variant
(splice donor variant)
Microcephaly and chorioretinopathy 2
GLikely pathogenic
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