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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF11
(G117C)
Single nucleotide variant
(missense variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GUncertain significance
KIF11
(Q781*)
Single nucleotide variant
(nonsense)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GPathogenic