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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USP9X
(R6C)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 99
GUncertain significance
USP9X
(A1830G +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 99
GUncertain significance
HUWE1
(R162G +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 99
GUncertain significance
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