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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNRC6B
(W680*)
Single nucleotide variant
(nonsense +1 more)
Global developmental delay with speech and behavioral abnormalities
GPathogenic
TNRC6B
(H1470P +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity