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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HUWE1
(A737V)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked syndromic, Turner type
GUncertain significance
BMX, CXorf38
+821 more
Copy number gain
Klinefelter syndrome
GPathogenic