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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNPO2
(L644fs)
Insertion
(frameshift variant +1 more)
Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
GLikely pathogenic
TNPO2
(K484N)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
GUncertain significance