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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZFHX4
(P40S)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
GUncertain significance
ZFHX4
(T1408fs)
Deletion
(frameshift variant)
Neurodevelopmental disorder
GLikely pathogenic
ZFHX4
(R1899*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder
GPathogenic
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