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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TLK2
(R190P +4 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 57
GUncertain significance
TLK2
(Q234* +5 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 57
GLikely pathogenic
TLK2
(R558C +5 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 57
GUncertain significance
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