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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEXMIF
(N1153fs)
Duplication
(frameshift variant)
not specified
+2 more
GPathogenic
NEXMIF
(Q1137*)
Single nucleotide variant
(nonsense)
X-linked intellectual disability, Cantagrel type
GPathogenic
NEXMIF
(E1042D)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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