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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLTC
(F37fs)
Deletion
(frameshift variant)
Intellectual disability, autosomal dominant 56
GLikely pathogenic
CLTC
(R63*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 56
+1 more
GPathogenic
CLTC
(Q531L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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