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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFIB
(R192* +5 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
NFIB
Single nucleotide variant
(splice donor variant +1 more)
Neurodevelopmental disorder
GUncertain significance