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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HUWE1
(S4287F)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked syndromic, Turner type
+1 more
GUncertain significance
HUWE1
(S2338T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance