| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ATXN2L, LOC130058734 (P18T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATXN2L, LOC130058734 (G37D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATXN2L, LOC130058734 (T44N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATXN2L, LOC130058734 (G30C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATXN2L, LOC130058734 (G75D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene