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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLTC
(S378L +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
+1 more
GUncertain significance
CLTC
(R1046H +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
+1 more
GUncertain significance