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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLTC
(S659* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 56
GPathogenic
CLTC
(P817fs +1 more)
Deletion
(frameshift variant)
Intellectual disability, autosomal dominant 56
GPathogenic
CLTC
(L1157* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 56
GPathogenic
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