| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126863207, MID1 (D630N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126863207, MID1 (S576F +1 more) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | LOC126863207, MID1 (I555V +1 more) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
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