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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHAMP1
(P159S)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 40
GUncertain significance
CHAMP1
(S308L)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 40
GUncertain significance
CHAMP1
(L451F)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 40
GUncertain significance
ABHD13, ADPRHL1
+56 more
Copy number gain
not provided
GPathogenic
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