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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEXMIF
(S1200fs)
Duplication
(frameshift variant)
X-linked intellectual disability, Cantagrel type
+1 more
GPathogenic
NEXMIF
(D1143H)
Single nucleotide variant
(missense variant)
X-linked intellectual disability, Cantagrel type
+1 more
GConflicting classifications of pathogenicity
NEXMIF
(R628*)
Single nucleotide variant
(nonsense)
X-linked intellectual disability, Cantagrel type
+2 more
GPathogenic
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