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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NKAP
(E124K)
Single nucleotide variant
(missense variant)
Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy
GUncertain significance
BMX, CXorf38
+821 more
Copy number gain
Klinefelter syndrome
GPathogenic