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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB39B
(V117L)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 72
GUncertain significance
RAB39B
(S22A)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 72
GUncertain significance