| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126863207, MID1 (T663I +1 more) | Single nucleotide variant (missense variant) | MID1-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | MID1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | LOC126863207, MID1 (A598V +1 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
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