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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USP9X
(P87fs)
Deletion
(frameshift variant)
Intellectual disability, X-linked 99
GPathogenic
USP9X
Single nucleotide variant
(intron variant)
Intellectual disability, X-linked 99, syndromic, female-restricted
GUncertain significance