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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MID2
(I103S +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 101
GUncertain significance
LOC101928335, MID2
(L349P +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 101
GUncertain significance
LOC101928335, MID2
(G520S +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 101
GConflicting classifications of pathogenicity
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