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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHM, LOC129391306
(E152* +1 more)
Duplication
(nonsense)
Choroideremia
GLikely pathogenic
BMX, CXorf38
+821 more
Copy number gain
Klinefelter syndrome
GPathogenic