| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DYM, DYM-AS1 (D418N +18 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | DYM, DYM-AS1 (G463S +18 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | DYM, DYM-AS1 (Y457C +18 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | DYM, DYM-AS1 (Y452C +18 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
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