| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Intellectual disability, X-linked 101 | |
| | LOC101928335, MID2 (L349P +1 more) | Single nucleotide variant (missense variant) | Intellectual disability, X-linked 101 | |
| | LOC101928335, MID2 (G520S +1 more) | Single nucleotide variant (missense variant) | Intellectual disability, X-linked 101 | GConflicting classifications of pathogenicity |
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