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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCX
(A295T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCX
Single nucleotide variant
(splice acceptor variant)
Lissencephaly type 1 due to doublecortin gene mutation
+1 more
GPathogenic/Likely pathogenic
DCX
(T121I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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