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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TUBGCP6
(G990R)
Single nucleotide variant
(missense variant)
Microcephaly and chorioretinopathy 1
GLikely pathogenic
TUBGCP6
(V359I)
Single nucleotide variant
(missense variant)
Microcephaly and chorioretinopathy 1
GLikely pathogenic