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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USP9X
(N15fs)
Deletion
(frameshift variant)
Intellectual disability, X-linked 99, syndromic, female-restricted
GPathogenic
USP9X
(S626N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
USP9X
(P1490L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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