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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP1B
(R1106* +1 more)
Single nucleotide variant
(nonsense)
Periventricular nodular heterotopia 9
GUncertain significance
MAP1B
(T1215I +1 more)
Single nucleotide variant
(missense variant)
Macrocephaly
+2 more
GUncertain significance