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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USP9X
(D1891H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
USP9X
(A2481fs)
Duplication
(frameshift variant +1 more)
Intellectual disability, X-linked 99
+3 more
GUncertain significance