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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDK5RAP2
(D1377Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 3, primary, autosomal recessive
Gnot provided
CDK5RAP2
(G138S)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 3, primary, autosomal recessive
+2 more
GConflicting classifications of pathogenicity