| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ZMYM4, ZMYM4-AS1 (R216I +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZMYM4, ZMYM4-AS1 (K153N +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZMYM4, ZMYM4-AS1 (D159G +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZMYM4-AS1, ZMYM4 (R185Q +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
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