| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | MAF, WWOX (S411del +1 more) | Deletion (inframe_deletion) | Developmental and epileptic encephalopathy, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Developmental and epileptic encephalopathy, 28 +2 more | |
| | | Single nucleotide variant (missense variant) | Ayme-Gripp syndrome | |
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