| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129999735, MNX1 (A174del) | Microsatellite (inframe deletion) | MNX1-related condition | |
| | LOC129999735, MNX1 (Y166H) | Single nucleotide variant (missense variant) | not provided +1 more | |
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