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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PI4KA
(F1851S +2 more)
Single nucleotide variant
(missense variant)
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis
GUncertain significance
PI4KA
(D1807N +2 more)
Single nucleotide variant
(missense variant)
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis
GUncertain significance