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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129937632, LOC129937633
+11 more
Copy number loss
Intellectual disability, autosomal dominant 47
GLikely pathogenic
IL20RB, IL20RB-AS1
+26 more
Copy number loss
Intellectual disability, autosomal dominant 47
GLikely pathogenic
A4GNT, ARMC8
+54 more
Copy number gain
not provided
GPathogenic
EPHB1, KY
+17 more
Copy number loss
Intellectual disability, autosomal dominant 47
GLikely pathogenic
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