| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (splice donor variant) | Wiedemann-Steiner syndrome | |
| | TTC36-AS1, KMT2A (R3704* +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
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