| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129999735, MNX1 (A173P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999735, MNX1 (A170G) | Single nucleotide variant (missense variant) | Currarino triad +2 more | |
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