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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCX
(Q261fs +1 more)
Deletion
(frameshift variant)
Abnormal cerebral morphology
GPathogenic
DCX
(R196H +1 more)
Single nucleotide variant
(missense variant)
Ectopic tissue
+3 more
GPathogenic
DCX
(R186H +1 more)
Single nucleotide variant
(missense variant)
Lissencephaly type 1 due to doublecortin gene mutation
+2 more
GConflicting classifications of pathogenicity
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