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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP152
Insertion
(nonsense)
Microcephaly 9, primary, autosomal recessive
GPathogenic
CEP152
(Q157fs)
Duplication
(frameshift variant)
Microcephaly 9, primary, autosomal recessive
+1 more
GPathogenic/Likely pathogenic