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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIO
(G27V)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly
GUncertain significance
TRIO
(R1982H)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly
GUncertain significance