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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB39B
(E187*)
Single nucleotide variant
(nonsense)
Intellectual disability, X-linked 72
GPathogenic
RAB39B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign