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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFIA
(R28* +2 more)
Indel
(nonsense)
not provided
GLikely pathogenic
NFIA
(K320fs +2 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder
GLikely pathogenic