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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MCPH1
(D668fs)
Deletion
(frameshift variant +1 more)
Microcephaly 1, primary, autosomal recessive
GLikely pathogenic
AGPAT5, ANGPT2
+15 more
Copy number loss
Autism
+7 more
GPathogenic
ERICH1, FBXO25
+11 more
Copy number loss
Intellectual disability
GPathogenic
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