| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ANKMY1, DUSP28 +1 more (S110L) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ANKMY1, DUSP28 +1 more (C114Y) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | DUSP28, LOC106783501 +1 more (A116V) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ANKMY1, DUSP28 +1 more (M1L +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ANKMY1, DUSP28 +1 more (R120P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ANKMY1, DUSP28 +1 more (R120Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | DUSP28, LOC106783501 (A129P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DUSP28, LOC106783501 (Q131R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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