| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (frameshift variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Tay-Sachs disease +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Tay-Sachs disease +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene