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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEXMIF
(N1169K)
Single nucleotide variant
(missense variant)
X-linked intellectual disability, Cantagrel type
GUncertain significance
NEXMIF
(N1153fs)
Duplication
(frameshift variant)
X-linked intellectual disability, Cantagrel type
+2 more
GPathogenic
NEXMIF
(L819F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NEXMIF
(H665Y)
Single nucleotide variant
(missense variant)
X-linked intellectual disability, Cantagrel type
GUncertain significance
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