| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | MYCBP2, MYCBP2-AS1 (V3888M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (A3886T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (I3851V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (I3836T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (T3813S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (Y3794C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (G3789A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (H3700R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (Q3625K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MYCBP2, MYCBP2-AS1 (N3583S) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
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