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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPL10
(S43T +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked, syndromic, 35
+1 more
GUncertain significance
ARHGAP4, ATP6AP1
+19 more
Copy number gain
Abnormal facial shape
+3 more
GPathogenic