| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130006629, MAML2 (G15V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861303, MAML2 (P799S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126861303, MAML2 (R792Q) | Single nucleotide variant (missense variant) | not specified | |
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