| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ASH1L, MIR555 (V2611L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ASH1L, MIR555 (P2625T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
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